6-57006887-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57006887
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57006887
    reference: chr 6
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-7874T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+8939T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1139A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.46-25542T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+8814T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.214-7874T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.998A>G
  hgvsp: ENSP00000359740.4:p.His333Arg
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.130-7874T>C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*85A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.998A>G
  hgvsp: ENSP00000350083.3:p.His333Arg
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.998A>G
  hgvsp: ENSP00000421645.1:p.His333Arg
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.46-26831T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-7874T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.444-26526T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-7874T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His333Arg
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff

6-57006893-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57006893
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57006893
    reference: chr 6
allele count: 1
allele frequency: 8.257638315441784e-6
allele num: 121100
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.444-26532C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-7880C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1004G>A
  hgvsp: ENSP00000421645.1:p.Arg335Lys
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1004G>A
  hgvsp: ENSP00000359740.4:p.Arg335Lys
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.130-7880C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.46-26837C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-7880C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1004G>A
  hgvsp: ENSP00000350083.3:p.Arg335Lys
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.46-25548C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.214-7880C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1145G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+8933C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+8808C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-7880C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg335Lys
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

6-57006894-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57006894
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57006894
    reference: chr 6
allele count: 1
allele frequency: 8.25722920416825e-6
allele num: 121106
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.46-25549C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.46-26838C>A
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1004+1G>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+1G>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+8807C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-7881C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.130-7881C>A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1004+1G>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-7881C>A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1145+1G>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.444-26533C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-7881C>A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1004+1G>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+8932C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.214-7881C>A
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43101
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1004+1G>T
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP

6-57006905-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57006905
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57006905
    reference: chr 6
allele count: 3
allele frequency: 2.479789713832267e-5
allele num: 120978
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.46-25560A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.130-7892A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-7892A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1004+12T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1004+12T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+8921A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+8796A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-7892A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.46-26849A>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.444-26544A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-7892A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.214-7892A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+12T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1004+12T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1145+12T>C
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

6-57006906-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57006906
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57006906
    reference: chr 6
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.444-26545G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-7893G>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+13C>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+8920G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1004+13C>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-7893G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1004+13C>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-7893G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.214-7893G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.46-25561G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+8795G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1145+13C>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.46-26850G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.130-7893G>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1004+13C>G
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

6-57006910-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57006910
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57006910
    reference: chr 6
allele count: 5
allele frequency: 4.134418204670239e-5
allele num: 120936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1004+17A>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-7897T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-7897T>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1004+17A>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+8791T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1004+17A>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+17A>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-7897T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+8916T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.46-25565T>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.444-26549T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.46-26854T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.130-7897T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1145+17A>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.214-7897T>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3989
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

6-57006914-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57006914
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57006914
    reference: chr 6
allele count: 1
allele frequency: 8.271572260455268e-6
allele num: 120896
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-7901C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+8787C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1004+21G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1004+21G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-7901C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+8912C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.444-26553C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.46-26858C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.46-25569C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+21G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-7901C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.214-7901C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1004+21G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1145+21G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.130-7901C>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

6-57006917-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57006917
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57006917
    reference: chr 6
allele count: 1
allele frequency: 8.271435424903638e-6
allele num: 120898
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1004+24A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-7904T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.444-26556T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1145+24A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.130-7904T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1004+24A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.46-25572T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-7904T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+8784T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1004+24A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.214-7904T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.46-26861T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-7904T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+24A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+8909T>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8786
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

6-57006925-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57006925
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57006925
    reference: chr 6
allele count: 3
allele frequency: 2.484760137821362e-5
allele num: 120736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-7912G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+32C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.214-7912G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1004+32C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.46-26869G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1004+32C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+8776G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1004+32C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.46-25580G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-7912G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+8901G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-7912G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.130-7912G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.444-26564G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1145+32C>T
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

6-57006926-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57006926
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57006926
    reference: chr 6
allele count: 1
allele frequency: 8.279516476237788e-6
allele num: 120780
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-7913C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.46-25581C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+33G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.214-7913C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1004+33G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.444-26565C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.46-26870C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1004+33G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.130-7913C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-7913C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+8775C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1145+33G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+8900C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1004+33G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-7913C>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8573
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum

6-57006929-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57006929
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57006929
    reference: chr 6
allele count: 34
allele frequency: 2.815315315315315e-4
allele num: 120768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-7916A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+8772A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.46-26873A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1004+36T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1004+36T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.214-7916A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.130-7916A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.46-25584A>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.444-26568A>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1004+36T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1145+36T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-7916A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+8897A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+36T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-7916A>G
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41245
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

6-57006933-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57006933
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57006933
    reference: chr 6
allele count: 27234
allele frequency: 2.257273104019892e-1
allele num: 120650
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.444-26572A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1004+40T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+8768A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-7920A>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1004+40T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+8893A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1145+40T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.46-25588A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1004+40T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.46-26877A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+40T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-7920A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-7920A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.130-7920A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.214-7920A>G
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.25e1
  variant carriers: 399
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 9.25e1
  variant carriers: 1287
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 5.75e1
  variant carriers: 479
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.75e1
  variant carriers: 301
genotype depth: GenotypeDepth
  all individuals: 5494
  bin: 2.75e1
  variant carriers: 556
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 1.25e1
  variant carriers: 224
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 1.75e1
  variant carriers: 553
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.75e1
  variant carriers: 705
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 7.75e1
  variant carriers: 927
genotype depth: GenotypeDepth
  all individuals: 25139
  bin: 2.25e1
  variant carriers: 694
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 8.25e1
  variant carriers: 1047
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 8.75e1
  variant carriers: 1171
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 7.25e1
  variant carriers: 789
genotype quality: GenotypeQuality
num of homozygotes: 3357
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

6-57006934-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57006934
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57006934
    reference: chr 6
allele count: 2
allele frequency: 1.659365458648613e-5
allele num: 120528
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+41G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1145+41G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-7921C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.46-26878C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.46-25589C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.444-26573C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-7921C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-7921C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1004+41G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+8767C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1004+41G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1004+41G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.214-7921C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.130-7921C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+8892C>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8182
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

6-57006936-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57006936
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57006936
    reference: chr 6
allele count: 2
allele frequency: 1.659255326209597e-5
allele num: 120536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-7923A>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.444-26575A>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1004+43T>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-7923A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.46-26880A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.214-7923A>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1004+43T>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1004+43T>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.46-25591A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+8890A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1145+43T>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+8765A>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+43T>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.130-7923A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-7923A>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8183
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

6-57006939-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57006939
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57006939
    reference: chr 6
allele count: 4
allele frequency: 3.326403326403326e-5
allele num: 120250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.214-7926G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1145+46C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.46-25594G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-7926G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+46C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+8887G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-7926G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1004+46C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-7926G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1004+46C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.444-26578G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.46-26883G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+8762G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.130-7926G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1004+46C>T
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8183
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

6-57006942-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57006942
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57006942
    reference: chr 6
allele count: 1
allele frequency: 8.316561600771776e-6
allele num: 120242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+8759C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.46-25597C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-7929C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-7929C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1145+49G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.444-26581C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.46-26886C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1004+49G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.214-7929C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+8884C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+49G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-7929C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.130-7929C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1004+49G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1004+49G>A
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/6-57011850-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011850
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011850
    reference: chr 6
allele count: 1
allele frequency: 1.23661365716123e-5
allele num: 80866
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3851G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12837G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23953G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1146-38C>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1005-38C>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3976G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3976G>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+4957C>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1005-38C>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1005-38C>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23953G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4771G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12837G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12837G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23953G>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2875
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10971
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17719
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16923
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

6-57011858-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011858
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011858
    reference: chr 6
allele count: 1
allele frequency: 1.197776926025297e-5
allele num: 83488
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1005-30A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+4965A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4763T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12845T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3843T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3968T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1146-30A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23945T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3968T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1005-30A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12845T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23945T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23945T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12845T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1005-30A>G
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13668
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16885
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

6-57011860-ACTTT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011860
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011856
    reference: chr 6
allele count: 13
allele frequency: 1.539773534846259e-4
allele num: 84428
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3962_213+3965delAAAG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1005-25_1005-22delTTCT
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12851_46-12848delAAAG
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+4970_*91+4973delTTCT
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12851_46-12848delAAAG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4757_129+4760delAAAG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1005-25_1005-22delTTCT
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12851_46-12848delAAAG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1146-25_1146-22delTTCT
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3962_213+3965delAAAG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23939_45+23942delAAAG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3837_257+3840delAAAG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23939_45+23942delAAAG
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1005-25_1005-22delTTCT
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23939_443+23942delAAAG
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19650
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12546
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16626
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: ACTTT
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

6-57011865-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011865
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011865
    reference: chr 6
allele count: 1
allele frequency: 1.146342022605865e-5
allele num: 87234
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3961G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12852G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23938G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1146-23C>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23938G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12852G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3836G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1005-23C>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23938G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3961G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1005-23C>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12852G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4756G>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+4972C>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1005-23C>G
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10082
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

6-57011867-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011867
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011867
    reference: chr 6
allele count: 6
allele frequency: 6.755387421468622e-5
allele num: 88818
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4754T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12854T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+4974A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3959T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1005-21A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1005-21A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23936T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3959T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1005-21A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1146-21A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3834T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12854T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23936T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23936T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12854T>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4815
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25169
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9063
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

6-57011873-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011873
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011873
    reference: chr 6
allele count: 1
allele frequency: 1.055074910318633e-5
allele num: 94780
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3953A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12860A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23930A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3953A>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+4980T>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12860A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3828A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1146-15T>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23930A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1005-15T>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4748A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12860A>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23930A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1005-15T>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1005-15T>G
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-57011876-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011876
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011877
    reference: chr 6
allele count: 1
allele frequency: 1.018620380556574e-5
allele num: 98172
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3949dupT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1005-11dupA
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23926dupT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12864dupT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23926dupT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12864dupT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23926dupT
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+4984dupA
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3949dupT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1146-11dupA
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1005-11dupA
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12864dupT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1005-11dupA
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4744dupT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3824dupT
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10884
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5798
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

6-57011879-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011879
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011879
    reference: chr 6
allele count: 1
allele frequency: 9.814313194362659e-6
allele num: 101892
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3822G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1005-9C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1005-9C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12866G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23924G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23924G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1005-9C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1146-9C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3947G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+4986C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23924G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3947G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12866G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4742G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12866G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3273
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9058
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36633
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-57011882-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011882
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011882
    reference: chr 6
allele count: 1
allele frequency: 9.463961235614779e-6
allele num: 105664
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23921T>C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1005-6A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12869T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23921T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23921T>C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1005-6A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+4989A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1146-6A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12869T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12869T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3944T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3944T>C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1005-6A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4739T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3819T>C
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38997
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1005-6A>G
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-57011892-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011892
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011892
    reference: chr 6
allele count: 1
allele frequency: 8.830022075055188e-6
allele num: 113250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3934G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1009C>T
  hgvsp: ENSP00000359740.4:p.His337Tyr
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1009C>T
  hgvsp: ENSP00000421645.1:p.His337Tyr
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1009C>T
  hgvsp: ENSP00000350083.3:p.His337Tyr
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3934G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12879G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4729G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12879G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23911G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12879G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1150C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23911G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23911G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+4999C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3809G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3859
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7516
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His337Tyr
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

6-57011898-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011898
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011898
    reference: chr 6
allele count: 1
allele frequency: 8.619500758516067e-6
allele num: 116016
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1015C>T
  hgvsp: ENSP00000359740.4:p.Arg339Ter
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23905G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3803G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12885G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23905G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5005C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12885G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4723G>A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1015C>T
  hgvsp: ENSP00000421645.1:p.Arg339Ter
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1015C>T
  hgvsp: ENSP00000350083.3:p.Arg339Ter
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23905G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3928G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1156C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12885G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3928G>A
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2537
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7988
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg339Ter
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ

6-57011899-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011899
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011899
    reference: chr 6
allele count: 4
allele frequency: 3.424540255470703e-5
allele num: 116804
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1157G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3802C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1016G>A
  hgvsp: ENSP00000350083.3:p.Arg339Gln
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12886C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1016G>A
  hgvsp: ENSP00000359740.4:p.Arg339Gln
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3927C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12886C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12886C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1016G>A
  hgvsp: ENSP00000421645.1:p.Arg339Gln
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3927C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23904C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4722C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23904C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23904C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5006G>A
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8139
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg339Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP

6-57011906-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011906
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011906
    reference: chr 6
allele count: 1
allele frequency: 8.433125316242199e-6
allele num: 118580
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23897A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23897A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12893A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3795A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1164T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3920A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3920A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12893A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1023T>C
  hgvsp: ENST00000491832.2:c.1023T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1023T>C
  hgvsp: ENST00000370706.4:c.1023T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4715A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12893A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5013T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23897A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1023T>C
  hgvsp: ENST00000357489.3:c.1023T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala341Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

6-57011912-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011912
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011912
    reference: chr 6
allele count: 1
allele frequency: 8.377875705836028e-6
allele num: 119362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23891A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3789A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1170T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23891A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12899A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23891A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1029T>C
  hgvsp: ENST00000357489.3:c.1029T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1029T>C
  hgvsp: ENST00000370706.4:c.1029T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3914A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1029T>C
  hgvsp: ENST00000491832.2:c.1029T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4709A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5019T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3914A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12899A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12899A>G
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8823
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro343Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

6-57011915-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011915
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011915
    reference: chr 6
allele count: 1
allele frequency: 8.354358468813179e-6
allele num: 119698
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5022A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1032A>G
  hgvsp: ENST00000357489.3:c.1032A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3911T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1032A>G
  hgvsp: ENST00000491832.2:c.1032A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3911T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12902T>C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1032A>G
  hgvsp: ENST00000370706.4:c.1032A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23888T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23888T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1173A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12902T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23888T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4706T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12902T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3786T>C
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val344Val
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

6-57011918-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011918
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011918
    reference: chr 6
allele count: 8
allele frequency: 6.666666666666667e-5
allele num: 120000
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3783A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4703A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12905A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3908A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23885A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1035T>C
  hgvsp: ENST00000491832.2:c.1035T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1176T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23885A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12905A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1035T>C
  hgvsp: ENST00000357489.3:c.1035T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23885A>G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1035T>C
  hgvsp: ENST00000370706.4:c.1035T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5025T>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3908A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12905A>G
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9059
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala345Ala
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

6-57011919-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011919
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011919
    reference: chr 6
allele count: 1
allele frequency: 8.327226700419692e-6
allele num: 120088
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3782C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4702C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1036G>A
  hgvsp: ENSP00000350083.3:p.Val346Ile
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23884C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1036G>A
  hgvsp: ENSP00000359740.4:p.Val346Ile
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12906C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3907C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23884C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23884C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1177G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5026G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3907C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1036G>A
  hgvsp: ENSP00000421645.1:p.Val346Ile
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12906C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12906C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45146
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val346Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

6-57011937-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011937
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011937
    reference: chr 6
allele count: 3
allele frequency: 2.481676951838923e-5
allele num: 120886
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12924T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3889T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3764T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12924T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5044A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1054A>G
  hgvsp: ENSP00000350083.3:p.Thr352Ala
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1054A>G
  hgvsp: ENSP00000421645.1:p.Thr352Ala
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1195A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3889T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4684T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23866T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1054A>G
  hgvsp: ENSP00000359740.4:p.Thr352Ala
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23866T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23866T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12924T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr352Ala
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-57011951-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011951
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011951
    reference: chr 6
allele count: 1
allele frequency: 8.256002113536541e-6
allele num: 121124
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1068G>T
  hgvsp: ENSP00000350083.3:p.Glu356Asp
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3875C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4670C>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23852C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3750C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12938C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23852C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1209G>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3875C>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1068G>T
  hgvsp: ENSP00000359740.4:p.Glu356Asp
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1068G>T
  hgvsp: ENSP00000421645.1:p.Glu356Asp
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12938C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12938C>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5058G>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23852C>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu356Asp
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

6-57011963-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011963
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011963
    reference: chr 6
allele count: 1
allele frequency: 8.25000825000825e-6
allele num: 121212
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23840T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1080A>G
  hgvsp: ENST00000491832.2:c.1080A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5070A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1080A>G
  hgvsp: ENST00000357489.3:c.1080A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1221A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3738T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12950T>C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1080A>G
  hgvsp: ENST00000370706.4:c.1080A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12950T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3863T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12950T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23840T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4658T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3863T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23840T>C
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu360Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

6-57011965-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011965
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011965
    reference: chr 6
allele count: 1
allele frequency: 8.249463784853985e-6
allele num: 121220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3861C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3736C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4656C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12952C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23838C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1082G>A
  hgvsp: ENSP00000421645.1:p.Arg361Lys
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3861C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5072G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1082G>A
  hgvsp: ENSP00000359740.4:p.Arg361Lys
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12952C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1082G>A
  hgvsp: ENSP00000350083.3:p.Arg361Lys
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23838C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12952C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23838C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1223G>A
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 9800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44939
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg361Lys
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

6-57011967-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011967
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011967
    reference: chr 6
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1084G>A
  hgvsp: ENSP00000359740.4:p.Gly362Ser
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4654C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23836C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1225G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1084G>A
  hgvsp: ENSP00000350083.3:p.Gly362Ser
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3734C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12954C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1084G>A
  hgvsp: ENSP00000421645.1:p.Gly362Ser
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3859C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23836C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23836C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3859C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5074G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12954C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12954C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly362Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

6-57011986-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011986
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011986
    reference: chr 6
allele count: 15
allele frequency: 1.236664633040381e-4
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3715T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23817T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4635T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1244A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1103A>G
  hgvsp: ENSP00000421645.1:p.Asn368Ser
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23817T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1103A>G
  hgvsp: ENSP00000350083.3:p.Asn368Ser
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12973T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12973T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3840T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1103A>G
  hgvsp: ENSP00000359740.4:p.Asn368Ser
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3840T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12973T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23817T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5093A>G
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn368Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

6-57011993-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011993
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011993
    reference: chr 6
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12980G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23810G>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1110C>G
  hgvsp: ENST00000357489.3:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12980G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12980G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3708G>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1110C>G
  hgvsp: ENST00000491832.2:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1251C>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3833G>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23810G>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23810G>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5100C>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3833G>C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1110C>G
  hgvsp: ENST00000370706.4:c.1110C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4628G>C
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9898
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val370Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

6-57011993-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011993
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011993
    reference: chr 6
allele count: 1
allele frequency: 8.243615319934711e-6
allele num: 121306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1110C>T
  hgvsp: ENST00000491832.2:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5100C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23810G>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1110C>T
  hgvsp: ENST00000370706.4:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12980G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12980G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4628G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23810G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23810G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3833G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1251C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1110C>T
  hgvsp: ENST00000357489.3:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3708G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3833G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12980G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val370Val
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

6-57011999-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57011999
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57011999
    reference: chr 6
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12986C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4622C>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1116G>T
  hgvsp: ENST00000491832.2:c.1116G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3827C>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1116G>T
  hgvsp: ENST00000370706.4:c.1116G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1116G>T
  hgvsp: ENST00000357489.3:c.1116G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3827C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1257G>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3702C>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23804C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12986C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23804C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12986C>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5106G>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23804C>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9908
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val372Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/6-57012007-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012007
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012007
    reference: chr 6
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23796G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3694G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3819G>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1124C>A
  hgvsp: ENSP00000359740.4:p.Thr375Asn
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1265C>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1124C>A
  hgvsp: ENSP00000421645.1:p.Thr375Asn
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1124C>A
  hgvsp: ENSP00000350083.3:p.Thr375Asn
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5114C>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12994G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12994G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4614G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12994G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23796G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23796G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3819G>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9914
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr375Asn
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP

6-57012009-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012009
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012009
    reference: chr 6
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12996T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1126A>G
  hgvsp: ENSP00000350083.3:p.Ser376Gly
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1126A>G
  hgvsp: ENSP00000421645.1:p.Ser376Gly
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1267A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3692T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23794T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3817T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5116A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23794T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3817T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4612T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1126A>G
  hgvsp: ENSP00000359740.4:p.Ser376Gly
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12996T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12996T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23794T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9918
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser376Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-57012012-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012012
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012012
    reference: chr 6
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4609T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3689T>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1129A>C
  hgvsp: ENSP00000421645.1:p.Thr377Pro
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3814T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1270A>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1129A>C
  hgvsp: ENSP00000359740.4:p.Thr377Pro
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1129A>C
  hgvsp: ENSP00000350083.3:p.Thr377Pro
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23791T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23791T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-12999T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23791T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3814T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-12999T>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5119A>C
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-12999T>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr377Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

6-57012017-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012017
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012017
    reference: chr 6
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1134A>G
  hgvsp: ENST00000357489.3:c.1134A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3684T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3809T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23786T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1275A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5124A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13004T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23786T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13004T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23786T>C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1134A>G
  hgvsp: ENST00000370706.4:c.1134A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1134A>G
  hgvsp: ENST00000491832.2:c.1134A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4604T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13004T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3809T>C
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln378Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

6-57012020-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012020
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012020
    reference: chr 6
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23783A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3806A>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1137T>A
  hgvsp: ENSP00000350083.3:p.Asn379Lys
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3681A>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1137T>A
  hgvsp: ENSP00000421645.1:p.Asn379Lys
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1278T>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4601A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3806A>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5127T>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13007A>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1137T>A
  hgvsp: ENSP00000359740.4:p.Asn379Lys
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13007A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13007A>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23783A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23783A>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9937
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn379Lys
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: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

6-57012021-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012021
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012021
    reference: chr 6
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13008G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1138C>T
  hgvsp: ENSP00000359740.4:p.His380Tyr
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1279C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5128C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1138C>T
  hgvsp: ENSP00000350083.3:p.His380Tyr
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13008G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3680G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3805G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23782G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3805G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4600G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13008G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1138C>T
  hgvsp: ENSP00000421645.1:p.His380Tyr
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23782G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23782G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His380Tyr
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum

6-57012036-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012036
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012036
    reference: chr 6
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13023C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1294G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1153G>A
  hgvsp: ENSP00000359740.4:p.Gly385Arg
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23767C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23767C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3665C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1153G>A
  hgvsp: ENSP00000350083.3:p.Gly385Arg
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3790C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1153G>A
  hgvsp: ENSP00000421645.1:p.Gly385Arg
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3790C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4585C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13023C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23767C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13023C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5143G>A
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44747
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly385Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ

6-57012048-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012048
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012048
    reference: chr 6
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13035G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5155C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4573G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13035G>A
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1165C>T
  hgvsp: ENSP00000359740.4:p.Arg389Ter
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1306C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1165C>T
  hgvsp: ENSP00000421645.1:p.Arg389Ter
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23755G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3778G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13035G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3653G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3778G>A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1165C>T
  hgvsp: ENSP00000350083.3:p.Arg389Ter
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23755G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23755G>A
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg389Ter
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

6-57012049-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012049
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012049
    reference: chr 6
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13036C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23754C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3652C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23754C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3777C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1166G>A
  hgvsp: ENSP00000421645.1:p.Arg389Gln
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13036C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5156G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3777C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4572C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1166G>A
  hgvsp: ENSP00000359740.4:p.Arg389Gln
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23754C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1166G>A
  hgvsp: ENSP00000350083.3:p.Arg389Gln
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1307G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13036C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg389Gln
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ

6-57012059-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012059
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012059
    reference: chr 6
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4562G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3767G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1317C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1176C>T
  hgvsp: ENST00000357489.3:c.1176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13046G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13046G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23744G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23744G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1176C>T
  hgvsp: ENST00000491832.2:c.1176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13046G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23744G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5166C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1176C>T
  hgvsp: ENST00000370706.4:c.1176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3767G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3642G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44694
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn392Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

6-57012085-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012085
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012085
    reference: chr 6
allele count: 3
allele frequency: 2.473166147301776e-5
allele num: 121302
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23718T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5192A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1202A>G
  hgvsp: ENSP00000359740.4:p.Tyr401Cys
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23718T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3741T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1202A>G
  hgvsp: ENSP00000350083.3:p.Tyr401Cys
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13072T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13072T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1202A>G
  hgvsp: ENSP00000421645.1:p.Tyr401Cys
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3741T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23718T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1343A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3616T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4536T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13072T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr401Cys
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

6-57012085-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012085
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012085
    reference: chr 6
allele count: 5
allele frequency: 4.121943578836293e-5
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13072T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3741T>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1202A>T
  hgvsp: ENSP00000350083.3:p.Tyr401Phe
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3741T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1343A>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13072T>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23718T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4536T>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1202A>T
  hgvsp: ENSP00000359740.4:p.Tyr401Phe
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13072T>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1202A>T
  hgvsp: ENSP00000421645.1:p.Tyr401Phe
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23718T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3616T>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23718T>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5192A>T
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr401Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

6-57012092-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012092
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012092
    reference: chr 6
allele count: 6
allele frequency: 4.947637503092273e-5
allele num: 121270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1350C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1209C>T
  hgvsp: ENST00000357489.3:c.1209C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4529G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3609G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3734G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3734G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23711G>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1209C>T
  hgvsp: ENST00000370706.4:c.1209C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1209C>T
  hgvsp: ENST00000491832.2:c.1209C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13079G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23711G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23711G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13079G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5199C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13079G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3094
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44500
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His403His
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

6-57012096-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012096
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012096
    reference: chr 6
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13083T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3605T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3730T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1213A>G
  hgvsp: ENSP00000421645.1:p.Ser405Gly
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5203A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23707T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13083T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1213A>G
  hgvsp: ENSP00000350083.3:p.Ser405Gly
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3730T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23707T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1213A>G
  hgvsp: ENSP00000359740.4:p.Ser405Gly
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13083T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23707T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4525T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1354A>G
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser405Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

6-57012098-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012098
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012098
    reference: chr 6
allele count: 4
allele frequency: 3.298969072164949e-5
allele num: 121250
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23705G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3728G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23705G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3603G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1356C>T
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1215C>T
  hgvsp: ENST00000370706.4:c.1215C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1215C>T
  hgvsp: ENST00000357489.3:c.1215C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13085G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13085G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1215C>T
  hgvsp: ENST00000491832.2:c.1215C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23705G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13085G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4523G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3728G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5205C>T
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser405Ser
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS

6-57012099-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012099
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012099
    reference: chr 6
allele count: 25
allele frequency: 2.061923692327994e-4
allele num: 121246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13086C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3602C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23704C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1216G>A
  hgvsp: ENSP00000421645.1:p.Glu406Lys
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5206G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3727C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1216G>A
  hgvsp: ENSP00000359740.4:p.Glu406Lys
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23704C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23704C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3727C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1357G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1216G>A
  hgvsp: ENSP00000350083.3:p.Glu406Lys
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13086C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13086C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4522C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9981
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Glu406Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

6-57012102-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012102
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012102
    reference: chr 6
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13089C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5209G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13089C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23701C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1219G>A
  hgvsp: ENSP00000421645.1:p.Gly407Arg
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4519C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13089C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1219G>A
  hgvsp: ENSP00000350083.3:p.Gly407Arg
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23701C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1219G>A
  hgvsp: ENSP00000359740.4:p.Gly407Arg
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1360G>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3724C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3599C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3724C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23701C>T
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9989
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly407Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-57012105-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012105
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012105
    reference: chr 6
allele count: 4
allele frequency: 3.299513321785036e-5
allele num: 121230
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3596T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23698T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3721T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23698T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13092T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5212A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3721T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1363A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13092T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1222A>G
  hgvsp: ENSP00000359740.4:p.Asn408Asp
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13092T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1222A>G
  hgvsp: ENSP00000421645.1:p.Asn408Asp
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1222A>G
  hgvsp: ENSP00000350083.3:p.Asn408Asp
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4516T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23698T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9991
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn408Asp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

6-57012130-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012130
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012130
    reference: chr 6
allele count: 52
allele frequency: 4.295603614915657e-4
allele num: 121054
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13117T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23673T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1388A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4491T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3696T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3696T>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23673T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1247A>G
  hgvsp: ENSP00000350083.3:p.His416Arg
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13117T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1247A>G
  hgvsp: ENSP00000421645.1:p.His416Arg
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1247A>G
  hgvsp: ENSP00000359740.4:p.His416Arg
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13117T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23673T>C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5237A>G
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3571T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43838
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.His416Arg
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

6-57012132-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012132
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012132
    reference: chr 6
allele count: 1
allele frequency: 8.261595148791329e-6
allele num: 121042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13119A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3569A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13119A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3694A>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5239T>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1249T>A
  hgvsp: ENSP00000350083.3:p.Leu417Ile
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1390T>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4489A>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1249T>A
  hgvsp: ENSP00000421645.1:p.Leu417Ile
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1249T>A
  hgvsp: ENSP00000359740.4:p.Leu417Ile
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23671A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23671A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13119A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23671A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3694A>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu417Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/6-57012148-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012148
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012148
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 120924
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  hgvsc: ENST00000370706.4:c.1265C>A
  hgvsp: ENSP00000359740.4:p.Ser422Ter
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1265C>A
  hgvsp: ENSP00000421645.1:p.Ser422Ter
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000416069.2:n.443+23655G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23655G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  hgvsc: ENST00000444273.2:n.1406C>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  hgvsc: ENST00000504603.1:c.*91+5255C>A
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000588811.1:n.213+3678G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586668.1:n.46-13135G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586053.1:n.213+3678G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000591553.1:n.129+4473G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000585792.1:n.46-13135G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000586432.1:n.46-13135G>T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  hgvsc: ENST00000357489.3:c.1265C>A
  hgvsp: ENSP00000350083.3:p.Ser422Ter
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592038.1:n.257+3553G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000592500.1:n.45+23655G>T
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43608
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser422Ter
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum

6-57012149-A-ACCTCTTAATATG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012149
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012161
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 120918
alternate allele: ACCTCTTAATATG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112200
  ensembl transcript: ENST00000444273
  gene symbol: ZNF451
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000588811
  gene symbol: RP11-203B9.4
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000425047
  ensembl transcript: ENST00000504603
  gene symbol: ZNF451
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000350083
  ensembl transcript: ENST00000357489
  gene symbol: ZNF451
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592038
  gene symbol: RP11-203B9.4
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000585792
  gene symbol: RP11-203B9.4
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586432
  gene symbol: RP11-203B9.4
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000592500
  gene symbol: RP11-203B9.4
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586668
  gene symbol: RP11-203B9.4
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000591553
  gene symbol: RP11-203B9.4
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000359740
  ensembl transcript: ENST00000370706
  gene symbol: ZNF451
  variant of: http://identifiers.org/hgnc/21091
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000586053
  gene symbol: RP11-203B9.4
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000416069
  gene symbol: RP11-203B9.4
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43621
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser422_Lys423insProLeuAsnMet
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD

6-57012150-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 57012150
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 57012150
    reference: chr 6
allele count: 1
allele frequency: 8.270477702792114e-6
allele num: 120912
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226803
  ensembl transcript: ENST00000587815
  gene symbol: RP11-203B9.4
  hgvsc: ENST00000587815.1:n.45+23653T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112200
  ensembl protein: ENSP00000421645
  ensembl transcript: ENST00000491832
  gene symbol: ZNF451
  hgvsc: ENST00000491832.2:c.1267A>G
  hgvsp: ENSP00000421645.1:p.Lys423Glu
  variant of: http://identifiers.org/hgnc/21091
canonical: true
consequence: missense
filter: PASS
hgvs: p.Lys423Glu
num of homozygotes: 0
reference allele: A

GenotypeDepth
all individuals: 9096
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 94
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1128
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 160
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 90
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1982
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2528
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43232
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 874
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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QD
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ReadPosRankSum
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MQ
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FS
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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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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

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

South Asian
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allele frequency: 0.0e0
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Other
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African
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allele frequency: 0.0e0
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Latino
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allele num: 11578
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.50558692779046e-5
allele num: 66584
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MQRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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DP
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FS
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MQ
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 1

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

European (Non-Finnish)
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allele num: 66570
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European (Finnish)
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Other
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East Asian
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African
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South Asian
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DP
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BaseQRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
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VQSLOD
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GenotypeDepth
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variant carriers: 0

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

South Asian
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Other
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East Asian
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Latino
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African
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allele frequency: 4.809542131589073e-4
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European (Finnish)
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ClippingRankSum
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BaseQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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MQRankSum
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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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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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variant carriers: 0

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

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66562
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African
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Latino
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East Asian
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Other
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MQ
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InbreedingCoeff
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VQSLOD
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FS
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ReadPosRankSum
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QD
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ClippingRankSum
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DP
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele num: 8654
num of homozygotes: 0

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

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

MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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QD
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FS
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ReadPosRankSum
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MQ
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66512
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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num of homozygotes: 0

East Asian
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allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

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

South Asian
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allele frequency: 6.216585851050602e-5
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MQRankSum
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DP
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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MQ
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66542
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16102
num of homozygotes: 0

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

East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

Other
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allele count: 0
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num of homozygotes: 0

ClippingRankSum
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InbreedingCoeff
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VQSLOD
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DP
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ReadPosRankSum
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MQ
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SIO_000300: 5.606e1

MQRankSum
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FS
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SIO_000300: 4.772e0

QD
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BaseQRankSum
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SIO_000300: -9.22e-1

GenotypeDepth
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variant carriers: 3

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
type: Population
allele count: 0
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num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728011059270779e-4
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 1
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allele num: 904
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.005891547432969e-5
allele num: 66536
num of homozygotes: 0

African
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allele count: 29
allele frequency: 2.791682710820177e-3
allele num: 10388
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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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ReadPosRankSum
type: SiteQuality
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DP
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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VQSLOD
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FS
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MQ
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QD
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GenotypeDepth
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variant carriers: 13198

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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allele frequency: 1.28498727735369e-1
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African
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Other
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South Asian
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European (Non-Finnish)
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allele frequency: 2.371237860428756e-1
allele num: 66518
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Latino
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allele frequency: 1.864948988414318e-1
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European (Finnish)
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allele frequency: 3.401937046004843e-1
allele num: 6608
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FS
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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QD
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MQRankSum
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MQ
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ClippingRankSum
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 15966
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
type: Population
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East Asian
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Latino
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African
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allele count: 1
allele frequency: 9.658103148541626e-5
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European (Non-Finnish)
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ReadPosRankSum
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MQRankSum
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MQ
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VQSLOD
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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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QD
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GenotypeDepth
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.008966720828068e-5
allele num: 66468
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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BaseQRankSum
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QD
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MQ
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FS
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InbreedingCoeff
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VQSLOD
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DP
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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European (Non-Finnish)
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allele frequency: 6.024640780793445e-5
allele num: 66394
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506387081224391e-5
allele num: 66384
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
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SIO_000300: 4.247e0

QD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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MQRankSum
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SIO_000300: 6.820000000000001e-1

ReadPosRankSum
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DP
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SIO_000300: 2.893067e6

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 44502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5742
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.34698275862069e-4
allele num: 7424
num of homozygotes: 0

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

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

MQRankSum
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DP
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FS
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SIO_000300: 0.0e0

MQ
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InbreedingCoeff
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QD
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: -9.13e-1

ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
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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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 45962
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European (Finnish)
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Latino
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African
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InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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MQ
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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Latino
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European (Non-Finnish)
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East Asian
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South Asian
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European (Finnish)
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QD
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VQSLOD
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DP
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InbreedingCoeff
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FS
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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MQ
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GenotypeDepth
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variant carriers: 0

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

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

Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 1.004621257785815e-4
allele num: 9954
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East Asian
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South Asian
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BaseQRankSum
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ReadPosRankSum
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FS
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MQ
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MQRankSum
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ClippingRankSum
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VQSLOD
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QD
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.522626225714112e-5
allele num: 65676
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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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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ClippingRankSum
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FS
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InbreedingCoeff
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MQRankSum
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MQ
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DP
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ReadPosRankSum
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QD
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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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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 count: 0
allele frequency: 0.0e0
allele num: 65928
num of homozygotes: 0

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

Latino
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allele frequency: 8.761170492377782e-5
allele num: 11414
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 4.539951573849879e-4
allele num: 6608
num of homozygotes: 0

Other
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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QD
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DP
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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African
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ReadPosRankSum
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MQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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QD
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FS
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MQ
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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South Asian
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Other
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East Asian
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European (Non-Finnish)
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QD
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MQRankSum
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FS
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQ
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InbreedingCoeff
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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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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: 66688
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South Asian
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African
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East Asian
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Other
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Latino
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European (Finnish)
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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DP
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FS
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InbreedingCoeff
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MQ
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ClippingRankSum
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VQSLOD
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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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African
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European (Finnish)
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MQ
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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DP
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MQRankSum
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FS
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Non-Finnish)
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MQ
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QD
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VQSLOD
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DP
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FS
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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Latino
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European (Non-Finnish)
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MQRankSum
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MQ
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FS
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QD
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ReadPosRankSum
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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East Asian
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Latino
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African
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European (Finnish)
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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FS
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MQ
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QD
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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South Asian
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InbreedingCoeff
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QD
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MQRankSum
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VQSLOD
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FS
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DP
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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DP
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FS
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MQRankSum
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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BaseQRankSum
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FS
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VQSLOD
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MQ
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InbreedingCoeff
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QD
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ClippingRankSum
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DP
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10402
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

Other
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ReadPosRankSum
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SIO_000300: 4.8e-1

InbreedingCoeff
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SIO_000300: -2.0e-4

BaseQRankSum
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SIO_000300: -5.38e0

QD
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VQSLOD
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ClippingRankSum
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MQ
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SIO_000300: 5.942e1

DP
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SIO_000300: 1.471714e6

FS
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SIO_000300: 3.566e0

MQRankSum
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SIO_000300: 5.88e-1

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

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

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

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

Other
type: Population
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

BaseQRankSum
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SIO_000300: -6.53e-1

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

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

South Asian
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allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

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

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

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

East Asian
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FS
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SIO_000300: 9.49e-1

ReadPosRankSum
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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QD
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DP
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GenotypeDepth
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variant carriers: 1

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

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

East Asian
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European (Non-Finnish)
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African
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South Asian
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InbreedingCoeff
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BaseQRankSum
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DP
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ReadPosRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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QD
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FS
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MQ
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

Latino
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num of homozygotes: 0

African
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European (Finnish)
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East Asian
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Other
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South Asian
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MQ
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DP
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InbreedingCoeff
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MQRankSum
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QD
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FS
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Non-Finnish)
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allele frequency: 2.998590662388677e-5
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num of homozygotes: 0

South Asian
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East Asian
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European (Finnish)
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QD
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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DP
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

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

European (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 num: 11558
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East Asian
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allele frequency: 0.0e0
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Other
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BaseQRankSum
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FS
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SIO_000300: 3.75e-1

ClippingRankSum
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SIO_000300: -1.314e0

DP
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VQSLOD
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MQRankSum
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MQ
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QD
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InbreedingCoeff
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SIO_000300: -2.0e-4

ReadPosRankSum
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SIO_000300: 9.360000000000001e-1

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

Latino
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allele count: 3
allele frequency: 2.596503375454388e-4
allele num: 11554
num of homozygotes: 0

Other
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allele count: 2
allele frequency: 2.217294900221729e-3
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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South Asian
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African
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allele count: 47
allele frequency: 4.587155963302753e-3
allele num: 10246
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

DP
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SIO_000300: 1.46779e6

BaseQRankSum
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SIO_000300: 4.16e-1

FS
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ReadPosRankSum
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QD
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VQSLOD
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ClippingRankSum
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SIO_000300: -2.67e-1

InbreedingCoeff
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SIO_000300: 1.17e-2

MQRankSum
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SIO_000300: 1.9e-2

MQ
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SIO_000300: 5.97e1

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

European (Finnish)
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allele frequency: 0.0e0
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African
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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 (Non-Finnish)
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allele count: 1
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South Asian
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Other
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InbreedingCoeff
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MQ
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FS
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QD
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MQRankSum
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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DP
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SIO_000300: 1.465801e6

ClippingRankSum
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SIO_000300: 5.28e-1

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

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

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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QD
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VQSLOD
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FS
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DP
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BaseQRankSum
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MQRankSum
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SIO_000300: -3.22e-1

ClippingRankSum
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SIO_000300: -3.22e-1

InbreedingCoeff
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SIO_000300: -3.0e-4

MQ
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SIO_000300: 3.912e1

ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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BaseQRankSum
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SIO_000300: -6.840000000000001e-1

ClippingRankSum
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InbreedingCoeff
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FS
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MQRankSum
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ReadPosRankSum
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MQ
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DP
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VQSLOD
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QD
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