11-71629961-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71629961
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71629961
    reference: chr 11
allele count: 1
allele frequency: 7.038288288288288e-5
allele num: 14208
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.157A>C
  hgvsp: ENST00000529513.1:c.157A>C(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.157A>C
  hgvsp: ENST00000533047.1:c.157A>C(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.157A>C
  hgvsp: ENST00000529844.1:c.157A>C(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.157A>C
  hgvsp: ENST00000534704.1:c.157A>C(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436725
  ensembl transcript: ENST00000532852
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000532852.1:c.43A>C
  hgvsp: ENST00000532852.1:c.43A>C(p.%3D)
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.250A>C
  hgvsp: ENST00000528511.2:c.250A>C(p.%3D)
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2857
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5576
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2304
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg84Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

11-71629970-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71629970
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71629970
    reference: chr 11
allele count: 3
allele frequency: 2.110595187842972e-4
allele num: 14214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.148C>T
  hgvsp: ENSP00000435060.1:p.Gln50Ter
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.148C>T
  hgvsp: ENSP00000436412.1:p.Gln50Ter
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.148C>T
  hgvsp: ENSP00000435620.1:p.Gln50Ter
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436725
  ensembl transcript: ENST00000532852
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000532852.1:c.34C>T
  hgvsp: ENSP00000436725.1:p.Gln12Ter
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.241C>T
  hgvsp: ENSP00000434508.2:p.Gln81Ter
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.148C>T
  hgvsp: ENSP00000433080.1:p.Gln50Ter
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.148C>T
  hgvsp: ENST00000528184.1:c.148C>T(p.%3D)
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3308
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gln81Ter
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

11-71629977-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71629977
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71629977
    reference: chr 11
allele count: 2
allele frequency: 1.40666760444507e-4
allele num: 14218
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.141A>G
  hgvsp: ENST00000528184.1:c.141A>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.141A>G
  hgvsp: ENST00000533047.1:c.141A>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.141A>G
  hgvsp: ENST00000534704.1:c.141A>G(p.%3D)
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.234A>G
  hgvsp: ENST00000528511.2:c.234A>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436725
  ensembl transcript: ENST00000532852
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000532852.1:c.27A>G
  hgvsp: ENST00000532852.1:c.27A>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.141A>G
  hgvsp: ENST00000529844.1:c.141A>G(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.141A>G
  hgvsp: ENST00000529513.1:c.141A>G(p.%3D)
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2277
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5591
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val78Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

11-71629992-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71629992
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71629992
    reference: chr 11
allele count: 1
allele frequency: 7.03135986499789e-5
allele num: 14222
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.126T>C
  hgvsp: ENST00000529844.1:c.126T>C(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.126T>C
  hgvsp: ENST00000528184.1:c.126T>C(p.%3D)
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.219T>C
  hgvsp: ENST00000528511.2:c.219T>C(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.126T>C
  hgvsp: ENST00000533047.1:c.126T>C(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.126T>C
  hgvsp: ENST00000529513.1:c.126T>C(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436725
  ensembl transcript: ENST00000532852
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000532852.1:c.12T>C
  hgvsp: ENST00000532852.1:c.12T>C(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.126T>C
  hgvsp: ENST00000534704.1:c.126T>C(p.%3D)
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2097
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser73Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS

11-71630041-TTTAGCAAGTTCTCTACAGGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71630041
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71630021
    reference: chr 11
allele count: 2
allele frequency: 1.408450704225352e-4
allele num: 14200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsp: ENSP00000435060.1:p.Tyr19Ter
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsp: ENSP00000436412.1:p.Tyr19Ter
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsp: ENSP00000433080.1:p.Tyr19Ter
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsp: ENSP00000435620.1:p.Tyr19Ter
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsp: ENSP00000435720.1:p.Tyr19Ter
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsp: ENSP00000434508.2:p.Tyr50Ter
canonical: true
consequence: stop gained
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1928
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr50Ter
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: TTTAGCAAGTTCTCTACAGGA
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

11-71630061-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71630061
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71630061
    reference: chr 11
allele count: 1
allele frequency: 7.095217823187172e-5
allele num: 14094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.57T>A
  hgvsp: ENSP00000435620.1:p.Tyr19Ter
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.57T>A
  hgvsp: ENSP00000433080.1:p.Tyr19Ter
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.150T>A
  hgvsp: ENSP00000434508.2:p.Tyr50Ter
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.57T>A
  hgvsp: ENSP00000435720.1:p.Tyr19Ter
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.57T>A
  hgvsp: ENSP00000436412.1:p.Tyr19Ter
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.57T>A
  hgvsp: ENSP00000435060.1:p.Tyr19Ter
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3264
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2805
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1852
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Tyr50Ter
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

11-71630073-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71630073
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71630073
    reference: chr 11
allele count: 1
allele frequency: 7.185972980741592e-5
allele num: 13916
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.46-1G>A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.46-1G>A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.46-1G>A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.46-1G>A
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.46-1G>A
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.139-1G>A
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1895
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5232
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
hgvs: c.139-1G>A
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

11-71630074-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71630074
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71630074
    reference: chr 11
allele count: 8
allele frequency: 5.752912411908529e-4
allele num: 13906
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.46-2A>C
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.139-2A>C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.46-2A>C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.46-2A>C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.46-2A>C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.46-2A>C
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 5217
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1907
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
hgvs: c.139-2A>C
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

11-71630079-AAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71630079
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71630077
    reference: chr 11
allele count: 1
allele frequency: 7.248477819657872e-5
allele num: 13796
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.46-9_46-8delCT
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.46-9_46-8delCT
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.46-9_46-8delCT
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.139-9_139-8delCT
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.46-9_46-8delCT
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.46-9_46-8delCT
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1924
  bin: 7.5e0
  variant carriers: 0
hgvs: c.139-9_139-8delCT
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: AAG
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/11-71630111-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71630111
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71630111
    reference: chr 11
allele count: 1
allele frequency: 7.649938800489595e-5
allele num: 13072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.46-39G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.46-39G>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.139-39G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.46-39G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.46-39G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.46-39G>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1900
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP

11-71630111-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71630111
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71630111
    reference: chr 11
allele count: 2
allele frequency: 1.529987760097919e-4
allele num: 13072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.46-39G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.46-39G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.46-39G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.46-39G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.139-39G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.46-39G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1900
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 689
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS

11-71630112-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71630112
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71630112
    reference: chr 11
allele count: 2
allele frequency: 1.527650473571647e-4
allele num: 13092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.46-40C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.46-40C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.46-40C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.139-40C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.46-40C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.46-40C>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1904
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 968
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2131
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

11-71630115-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71630115
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71630115
    reference: chr 11
allele count: 1
allele frequency: 7.689941556444171e-5
allele num: 13004
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.46-43G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.46-43G>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.139-43G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.46-43G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.46-43G>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.46-43G>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 930
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1927
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1804
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ

11-71634305-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71634305
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71634305
    reference: chr 11
allele count: 15
allele frequency: 1.056933483652762e-3
allele num: 14192
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.45+50G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.139-4233G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.45+50G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.45+50G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.45+50G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.45+50G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1194
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4126
  bin: 9.75e1
  variant carriers: 15
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

11-71634344-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71634344
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71634344
    reference: chr 11
allele count: 46
allele frequency: 3.23943661971831e-3
allele num: 14200
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.45+11C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.45+11C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.139-4272C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.45+11C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.45+11C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.45+11C>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1010
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4143
  bin: 9.75e1
  variant carriers: 40
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1400
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 4
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/11-71634375-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71634375
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71634375
    reference: chr 11
allele count: 2
allele frequency: 1.407459535538353e-4
allele num: 14210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.25G>T
  hgvsp: ENSP00000433080.1:p.Val9Leu
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.25G>T
  hgvsp: ENSP00000435060.1:p.Val9Leu
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.25G>T
  hgvsp: ENSP00000435720.1:p.Val9Leu
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.25G>T
  hgvsp: ENSP00000435620.1:p.Val9Leu
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.25G>T
  hgvsp: ENSP00000436412.1:p.Val9Leu
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.139-4303G>T
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val9Leu
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

11-71634400-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71634400
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71634400
    reference: chr 11
allele count: 4
allele frequency: 2.814919071076706e-4
allele num: 14210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.-1C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.-1C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.-1C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.139-4328C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.-1C>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.-1C>T
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

11-71634426-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71634426
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71634426
    reference: chr 11
allele count: 5
allele frequency: 3.519144144144144e-4
allele num: 14208
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.-27G>C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.-27G>C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.-27G>C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.-27G>C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000436412
  ensembl transcript: ENST00000534704
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000534704.1:c.-27G>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.139-4354G>C
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-71639457-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71639457
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71639457
    reference: chr 11
allele count: 7
allele frequency: 6.93069306930693e-4
allele num: 10100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435060
  ensembl transcript: ENST00000529513
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529513.1:c.-169G>T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.-169G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254469
  ensembl transcript: ENST00000531488
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000531488.1:n.37G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.-295+38G>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.138+38G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.-123+38G>T
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2820
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2092
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

11-71639484-GGCCTTCTGACCTTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71639484
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71639470
    reference: chr 11
allele count: 1
allele frequency: 9.389671361502347e-5
allele num: 10650
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: 5_prime_UTR_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000254469
  ensembl transcript: ENST00000531488
  gene symbol: RP11-849H4.2
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  consequence: coding_sequence_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: 5_prime_UTR_variant
  consequence: intron_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
canonical: true
consequence: splice donor
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2289
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
hgvs: c.135_138+10delGAAGGTCAGAAGGC
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: GGCCTTCTGACCTTC
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

11-71639583-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71639583
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71639583
    reference: chr 11
allele count: 6
allele frequency: 5.574136008918618e-4
allele num: 10764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.-211T>C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.-295T>C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.-383T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.50T>C
  hgvsp: ENSP00000434508.2:p.Ile17Thr
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2110
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 4495
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile17Thr
num of homozygotes: 1
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

11-71639610-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71639610
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71639610
    reference: chr 11
allele count: 1
allele frequency: 9.291953168556031e-5
allele num: 10762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435620
  ensembl transcript: ENST00000533047
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000533047.1:c.-238C>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000435720
  ensembl transcript: ENST00000528184
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528184.1:c.-410C>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000434508
  ensembl transcript: ENST00000528511
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000528511.2:c.23C>G
  hgvsp: ENSP00000434508.2:p.Thr8Ser
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.-322C>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1951
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4489
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr8Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

11-71639671-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71639671
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71639671
    reference: chr 11
allele count: 3
allele frequency: 2.857687178510192e-4
allele num: 10498
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.-383A>C
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2787
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2134
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2237
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 9.75e1
  variant carriers: 3
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7356
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 134
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 118
  num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

11-71639677-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71639677
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71639677
    reference: chr 11
allele count: 8
allele frequency: 7.695267410542517e-4
allele num: 10396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.-389C>A
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 2274
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 563
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 8
  allele frequency: 1.098901098901099e-3
  allele num: 7280
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 118
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 188
  num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

11-71639679-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71639679
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71639679
    reference: chr 11
allele count: 1
allele frequency: 9.67305088024763e-5
allele num: 10338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000254469
  ensembl protein: ENSP00000433080
  ensembl transcript: ENST00000529844
  gene symbol: RP11-849H4.2
  hgvsc: ENST00000529844.1:c.-391C>T
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2233
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2574
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 186
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: NaN
  allele num: 0
  num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

11-71640064-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640064
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640064
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 20596
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.-44A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.-44A>G
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20095
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7318
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1177
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12673
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1749
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 797
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 825
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3318
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 8714
  num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

11-71640065-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640065
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640065
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 20586
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.-43G>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.-43G>T
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19968
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7358
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 797
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3318
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1711
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12507
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 1174
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2738
  num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

11-71640066-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640066
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640066
    reference: chr 11
allele count: 21
allele frequency: 1.019912578921807e-3
allele num: 20590
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.-42C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.-42C>T
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20022
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 304
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  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 12746
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 814
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 3329
  bin: 9.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 479
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 512
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1746
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 28
  num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

11-71640070-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640070
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640070
    reference: chr 11
allele count: 283
allele frequency: 1.37378640776699e-2
allele num: 20600
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.-38C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.-38C>T
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 2.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 19920
  bin: 2.5e0
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 2.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 9.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 3.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 3.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6582
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1783
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 1.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 13251
  bin: 7.5e0
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1152
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3432
  bin: 9.75e1
  variant carriers: 280
num of homozygotes: 2
population: Other
  type: Population
  allele count: 4
  allele frequency: 2.02020202020202e-2
  allele num: 198
  num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

11-71640071-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640071
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640071
    reference: chr 11
allele count: 20
allele frequency: 9.711566475672526e-4
allele num: 20594
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.-37T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.-37T>C
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19970
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1179
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6601
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1777
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 829
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13281
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3249
  bin: 9.75e1
  variant carriers: 20
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 30
  num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum

11-71640079-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640079
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640079
    reference: chr 11
allele count: 1
allele frequency: 4.828585224529213e-5
allele num: 20710
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.-87G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.-29G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.-29G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.-87G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.-29G>C
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21082
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1898
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1253
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4907
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16070
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-71640085-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640085
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640085
    reference: chr 11
allele count: 1
allele frequency: 6.066488716330988e-5
allele num: 16484
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.-81C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.-23C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.-81C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.-23C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.-23C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.-81C>T
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21718
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7015
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1999
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16651
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

11-71640086-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640086
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640086
    reference: chr 11
allele count: 6
allele frequency: 2.885170225043277e-4
allele num: 20796
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.-80G>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.-80G>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.-80G>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.-22G>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.-22G>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.-22G>T
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17660
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1471
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1014
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4310
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-71640088-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640088
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640088
    reference: chr 11
allele count: 1
allele frequency: 8.084074373484237e-5
allele num: 12370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.-78T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.-20T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.-78T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.-20T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.-20T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.-78T>G
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21863
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9638
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16166
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-71640090-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640090
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640090
    reference: chr 11
allele count: 10
allele frequency: 1.131990038487661e-3
allele num: 8834
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.-76A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.-18A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.-76A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.-76A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.-18A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.-18A>G
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: 5' UTR
filter: VQSRTrancheINDEL99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 22155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1593
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 11278
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16731
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 797
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ

11-71640093-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640093
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640093
    reference: chr 11
allele count: 1
allele frequency: 4.785604900459418e-5
allele num: 20896
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.-73G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.-15G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.-15G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.-73G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.-73G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.-15G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.2G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.1G>C
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23831
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

11-71640096-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640096
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640096
    reference: chr 11
allele count: 16
allele frequency: 2.600780234070221e-3
allele num: 6152
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.-70C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.-70C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.-70C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.5C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.-12C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.-12C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.4C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.-12C>G
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23056
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13616
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

11-71640096-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640096
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640096
    reference: chr 11
allele count: 4
allele frequency: 6.501950585175553e-4
allele num: 6152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.-70C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.-70C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.-12C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.-12C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.5C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.-70C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.4C>T
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: 5' UTR
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23056
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13616
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

11-71640107-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640107
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640107
    reference: chr 11
allele count: 3
allele frequency: 1.438710915020142e-4
allele num: 20852
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.-59G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.-1G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.15G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.-59G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.-59G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.-1G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.16G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.-59G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.-1G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-344G>A
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27210
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1113
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24681
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

11-71640112-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640112
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640112
    reference: chr 11
allele count: 2
allele frequency: 9.596928982725528e-5
allele num: 20840
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.21C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-339C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.-54C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.-54C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.5C>T
  hgvsp: ENSP00000354571.3:p.Ala2Val
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.-54C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.5C>T
  hgvsp: ENSP00000431325.1:p.Ala2Val
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.5C>T
  hgvsp: ENSP00000377314.3:p.Ala2Val
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.20C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.-54C>T
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27864
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala2Val
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

11-71640118-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640118
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640118
    reference: chr 11
allele count: 1
allele frequency: 4.803996925441968e-5
allele num: 20816
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.11T>C
  hgvsp: ENSP00000377314.3:p.Val4Ala
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.-48T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.27T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-333T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.-48T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.-48T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.11T>C
  hgvsp: ENSP00000354571.3:p.Val4Ala
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.-48T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.26T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.11T>C
  hgvsp: ENSP00000431325.1:p.Val4Ala
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28762
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val4Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ

11-71640133-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640133
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640133
    reference: chr 11
allele count: 1
allele frequency: 4.814172925091469e-5
allele num: 20772
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.26T>C
  hgvsp: ENSP00000377314.3:p.Val9Ala
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.-33T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.42T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.-33T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.-33T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.-33T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.26T>C
  hgvsp: ENSP00000354571.3:p.Val9Ala
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.41T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.12T>C
  hgvsp: ENSP00000435859.1:p.Val5Ala
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.26T>C
  hgvsp: ENSP00000431325.1:p.Val9Ala
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.-33T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-318T>C
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30587
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val9Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

11-71640137-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640137
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640137
    reference: chr 11
allele count: 2
allele frequency: 9.632055480639569e-5
allele num: 20764
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.30A>G
  hgvsp: ENST00000361756.3:c.30A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.30A>G
  hgvsp: ENST00000393711.3:c.30A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.-29A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.-29A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.16A>G
  hgvsp: ENST00000525243.1:c.16A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.30A>G
  hgvsp: ENST00000530058.1:c.30A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.46A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.45A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.-29A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.-29A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.-29A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-314A>G
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31036
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2802
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly10Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

11-71640145-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640145
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640145
    reference: chr 11
allele count: 1
allele frequency: 4.844961240310077e-5
allele num: 20640
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.38C>T
  hgvsp: ENSP00000431325.1:p.Ala13Val
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-306C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.38C>T
  hgvsp: ENSP00000377314.3:p.Ala13Val
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.38C>T
  hgvsp: ENSP00000354571.3:p.Ala13Val
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.24C>T
  hgvsp: ENSP00000435859.1:p.Ala9Val
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.54C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.-21C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.53C>T
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31297
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala13Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-71640148-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640148
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640148
    reference: chr 11
allele count: 1
allele frequency: 4.851072086931212e-5
allele num: 20614
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.41C>T
  hgvsp: ENSP00000354571.3:p.Ala14Val
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.41C>T
  hgvsp: ENSP00000377314.3:p.Ala14Val
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.-18C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.-18C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.-18C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-303C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.-18C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.27C>T
  hgvsp: ENSP00000435859.1:p.Ala10Val
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.56C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.-18C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.57C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.41C>T
  hgvsp: ENSP00000431325.1:p.Ala14Val
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31395
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3061
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala14Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD

11-71640155-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640155
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640155
    reference: chr 11
allele count: 1
allele frequency: 4.875670404680644e-5
allele num: 20510
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-296A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.48A>G
  hgvsp: ENST00000361756.3:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.63A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.48A>G
  hgvsp: ENST00000393711.3:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.34A>G
  hgvsp: ENST00000525243.1:c.34A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.-11A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.48A>G
  hgvsp: ENST00000530058.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.64A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.-11A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.-11A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.-11A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.-11A>G
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31422
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu16Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

11-71640167-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640167
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640167
    reference: chr 11
allele count: 5
allele frequency: 2.474512521033356e-4
allele num: 20206
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.60T>G
  hgvsp: ENSP00000431325.1:p.Asp20Glu
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.60T>G
  hgvsp: ENSP00000377314.3:p.Asp20Glu
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.2T>G
  hgvsp: ENSP00000431286.1:p.Met1?
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-284T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.2T>G
  hgvsp: ENSP00000377316.3:p.Met1?
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.2T>G
  hgvsp: ENSP00000432898.1:p.Met1?
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: start_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.2T>G
  hgvsp: ENSP00000434127.1:p.Met1?
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.2T>G
  hgvsp: ENSP00000433574.1:p.Met1?
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.75T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.60T>G
  hgvsp: ENSP00000354571.3:p.Asp20Glu
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.76T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.46T>G
  hgvsp: ENSP00000435859.1:p.Asp16Glu
  variant of: http://identifiers.org/hgnc/21070
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31015
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

11-71640172-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640172
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640172
    reference: chr 11
allele count: 1
allele frequency: 4.993508439029262e-5
allele num: 20026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-281+2T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.5+2T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.49+2T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.78+2T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.5+2T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.5+2T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.79+2T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.63+2T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.63+2T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.5+2T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.63+2T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.5+2T>C
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30618
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2104
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.63+2T>C
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

11-71640187-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640187
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640187
    reference: chr 11
allele count: 1
allele frequency: 5.140331037318804e-5
allele num: 19454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.5+17G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.63+17G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.5+17G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.78+17G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.5+17G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-281+17G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.79+17G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.5+17G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.63+17G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.5+17G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.63+17G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.49+17G>A
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29030
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD

11-71640193-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640193
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640193
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 19308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.5+23G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.5+23G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.79+23G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.63+23G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.78+23G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.5+23G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-281+23G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.63+23G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.63+23G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.5+23G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.49+23G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.5+23G>A
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28975
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

11-71640219-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71640219
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71640219
    reference: chr 11
allele count: 1
allele frequency: 5.572272372673576e-5
allele num: 17946
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.49+49A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.79+49A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.5+49A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.78+49A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.5+49A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.63+49A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.5+49A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-281+49A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.5+49A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.5+49A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.63+49A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.63+49A>T
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27257
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

11-71668224-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668224
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668224
    reference: chr 11
allele count: 1
allele frequency: 8.26255081468751e-6
allele num: 121028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3572G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3572G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.50-49G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3572G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.80-49G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.79-49G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.64-49G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.64-49G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.64-49G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3572G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3572G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3572G>A
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4668
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7199
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7486
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3709
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6919
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5686
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6116
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2352
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

11-71668226-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668226
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668226
    reference: chr 11
allele count: 538
allele frequency: 4.799543240494585e-3
allele num: 112094
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3570A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3570A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.50-47A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3570A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.64-47A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.64-47A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3570A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3570A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.79-47A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.64-47A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3570A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.80-47A>G
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7081
  bin: 5.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 4667
  bin: 9.75e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 3.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 2.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 3.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 2.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5975
  bin: 4.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 7.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 7110
  bin: 6.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 4028
  bin: 4.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 7517
  bin: 5.75e1
  variant carriers: 48
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-71668227-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668227
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668227
    reference: chr 11
allele count: 1
allele frequency: 8.287475966319697e-6
allele num: 120664
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3569C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3569C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.64-46C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.64-46C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.79-46C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3569C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3569C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3569C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3569C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.80-46C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.64-46C>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.50-46C>G
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7063
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5903
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3978
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7105
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7554
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

11-71668230-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668230
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668230
    reference: chr 11
allele count: 3
allele frequency: 2.481964392084188e-5
allele num: 120872
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.64-43T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.50-43T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.79-43T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3566T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3566T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3566T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3566T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.64-43T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3566T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3566T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.80-43T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.64-43T>G
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 5911
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5829
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4521
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ

11-71668232-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668232
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668232
    reference: chr 11
allele count: 1
allele frequency: 8.262277744728666e-6
allele num: 121032
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3564T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.64-41T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.80-41T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.79-41T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.64-41T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3564T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.64-41T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3564T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3564T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.50-41T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3564T>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3564T>G
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4523
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7563
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7058
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7105
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

11-71668234-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668234
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668234
    reference: chr 11
allele count: 3
allele frequency: 2.480979159775058e-5
allele num: 120920
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.79-39A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.64-39A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3562A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.64-39A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.64-39A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3562A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3562A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3562A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3562A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3562A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.80-39A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.50-39A>T
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4005
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7564
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5831
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7059
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5907
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP

11-71668277-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668277
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668277
    reference: chr 11
allele count: 3
allele frequency: 2.47137325974133e-5
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3519A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.68A>G
  hgvsp: ENSP00000431325.1:p.Asp23Gly
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.68A>G
  hgvsp: ENSP00000354571.3:p.Asp23Gly
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.68A>G
  hgvsp: ENSP00000377314.3:p.Asp23Gly
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3519A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3519A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.54A>G
  hgvsp: ENSP00000435859.1:p.Asp19Gly
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3519A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.83A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3519A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.84A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3519A>G
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp23Gly
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP

11-71668277-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668277
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668277
    reference: chr 11
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3519A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.68A>T
  hgvsp: ENSP00000377314.3:p.Asp23Val
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.54A>T
  hgvsp: ENSP00000435859.1:p.Asp19Val
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3519A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3519A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3519A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3519A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3519A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.68A>T
  hgvsp: ENSP00000354571.3:p.Asp23Val
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.84A>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.68A>T
  hgvsp: ENSP00000431325.1:p.Asp23Val
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.83A>T
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4526
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5850
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp23Val
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

11-71668281-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668281
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668281
    reference: chr 11
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.58G>C
  hgvsp: ENSP00000435859.1:p.Met20Ile
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3515G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.88G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.87G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3515G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.72G>C
  hgvsp: ENSP00000431325.1:p.Met24Ile
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3515G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.72G>C
  hgvsp: ENSP00000377314.3:p.Met24Ile
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.72G>C
  hgvsp: ENSP00000354571.3:p.Met24Ile
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3515G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3515G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3515G>C
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5852
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met24Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff

11-71668285-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668285
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668285
    reference: chr 11
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.76G>C
  hgvsp: ENSP00000354571.3:p.Asp26His
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3511G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.91G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.62G>C
  hgvsp: ENSP00000435859.1:p.Asp22His
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3511G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.76G>C
  hgvsp: ENSP00000377314.3:p.Asp26His
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000526903
  gene symbol: RNF121
  hgvsc: ENST00000526903.1:n.1G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3511G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.76G>C
  hgvsp: ENSP00000431325.1:p.Asp26His
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3511G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3511G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3511G>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.92G>C
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7056
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7123
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7567
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4476
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5852
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp26His
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

11-71668290-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668290
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668290
    reference: chr 11
allele count: 36
allele frequency: 2.965599051008304e-4
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3506C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000526903
  gene symbol: RNF121
  hgvsc: ENST00000526903.1:n.6C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.81C>T
  hgvsp: ENST00000530058.1:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.81C>T
  hgvsp: ENST00000361756.3:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3506C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3506C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.96C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.67C>T
  hgvsp: ENST00000525243.1:c.67C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.81C>T
  hgvsp: ENST00000393711.3:c.81C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.97C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3506C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3506C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3506C>T
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5849
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7052
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7560
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7116
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu27Leu
num of homozygotes: 1
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

11-71668305-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668305
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668305
    reference: chr 11
allele count: 1156
allele frequency: 9.522554285149429e-3
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.111A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3491A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3491A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.112A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3491A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3491A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.82A>G
  hgvsp: ENST00000525243.1:c.82A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3491A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.96A>G
  hgvsp: ENST00000361756.3:c.96A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.96A>G
  hgvsp: ENST00000393711.3:c.96A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000526903
  gene symbol: RNF121
  hgvsc: ENST00000526903.1:n.21A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3491A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.96A>G
  hgvsp: ENST00000530058.1:c.96A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7425
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 8.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7015
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5791
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6930
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 7.75e1
  variant carriers: 32
genotype quality: GenotypeQuality
hgvs: p.Gln32Gln
num of homozygotes: 8
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/11-71668309-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668309
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668309
    reference: chr 11
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.116A>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.86A>C
  hgvsp: ENST00000525243.1:c.86A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3487A>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.115A>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3487A>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3487A>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.100A>C
  hgvsp: ENST00000361756.3:c.100A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.100A>C
  hgvsp: ENST00000530058.1:c.100A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3487A>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000526903
  gene symbol: RNF121
  hgvsc: ENST00000526903.1:n.25A>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3487A>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3487A>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.100A>C
  hgvsp: ENST00000393711.3:c.100A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7127
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7017
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7536
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5863
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.100A>C
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP

11-71668315-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668315
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668315
    reference: chr 11
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.101+5G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3481G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.117+5G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.101+5G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3481G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.116+5G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.87+5G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3481G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3481G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3481G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000526903
  gene symbol: RNF121
  hgvsc: ENST00000526903.1:n.26+5G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.101+5G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3481G>A
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3960
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.101+5G>A
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-71668317-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668317
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668317
    reference: chr 11
allele count: 60
allele frequency: 4.942665085013839e-4
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.101+7G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3479G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3479G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3479G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.117+7G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000526903
  gene symbol: RNF121
  hgvsc: ENST00000526903.1:n.26+7G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.101+7G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3479G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.87+7G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.116+7G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3479G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3479G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.101+7G>A
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7016
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7119
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3956
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7524
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: c.101+7G>A
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

11-71668326-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668326
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668326
    reference: chr 11
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000526903
  gene symbol: RNF121
  hgvsc: ENST00000526903.1:n.26+16C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3470C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.101+16C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.101+16C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3470C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3470C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.87+16C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.101+16C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3470C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.117+16C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.116+16C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3470C>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3470C>T
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7530
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4536
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4562
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7016
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

11-71668328-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668328
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668328
    reference: chr 11
allele count: 115
allele frequency: 9.473597495675097e-4
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3468G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3468G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000526903
  gene symbol: RNF121
  hgvsc: ENST00000526903.1:n.26+18G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3468G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.87+18G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.101+18G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3468G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.101+18G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3468G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.116+18G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.117+18G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.101+18G>A
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3468G>A
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4532
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4596
  bin: 9.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 3191
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5885
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7011
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7124
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7522
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ

11-71668340-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668340
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668340
    reference: chr 11
allele count: 13
allele frequency: 1.071334388185654e-4
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.116+30T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.101+30T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3456T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3456T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3456T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3456T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.87+30T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.101+30T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3456T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3456T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.117+30T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.101+30T>C
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000526903
  gene symbol: RNF121
  hgvsc: ENST00000526903.1:n.26+30T>C
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4566
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5809
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7519
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6981
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4535
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP

11-71668344-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668344
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668344
    reference: chr 11
allele count: 7
allele frequency: 5.771196781321109e-5
allele num: 121292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3452A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000528683
  gene symbol: RNF121
  hgvsc: ENST00000528683.1:n.116+34A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3452A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000432898
  ensembl transcript: ENST00000530655
  gene symbol: RNF121
  hgvsc: ENST00000530655.1:c.6-3452A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377314
  ensembl transcript: ENST00000393711
  gene symbol: RNF121
  hgvsc: ENST00000393711.3:c.101+34A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000354571
  ensembl transcript: ENST00000361756
  gene symbol: RNF121
  hgvsc: ENST00000361756.3:c.101+34A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000434127
  ensembl transcript: ENST00000526549
  gene symbol: RNF121
  hgvsc: ENST00000526549.1:c.6-3452A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000377316
  ensembl transcript: ENST00000393713
  gene symbol: RNF121
  hgvsc: ENST00000393713.3:c.6-3452A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000490867
  gene symbol: RNF121
  hgvsc: ENST00000490867.1:n.117+34A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000435859
  ensembl transcript: ENST00000525243
  gene symbol: RNF121
  hgvsc: ENST00000525243.1:c.87+34A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.101+34A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000433574
  ensembl transcript: ENST00000533380
  gene symbol: RNF121
  hgvsc: ENST00000533380.1:c.6-3452A>G
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000526903
  gene symbol: RNF121
  hgvsc: ENST00000526903.1:n.26+34A>G
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5863
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7073
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7506
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4530
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

11-71668348-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71668348
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71668348
    reference: chr 11
allele count: 6
allele frequency: 4.96310756708467e-5
allele num: 120892
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000443799
  ensembl transcript: ENST00000545854
  gene symbol: RNF121
  hgvsc: ENST00000545854.1:c.-280-3448G>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431325
  ensembl transcript: ENST00000530058
  gene symbol: RNF121
  hgvsc: ENST00000530058.1:c.101+38G>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl transcript: ENST00000526903
  gene symbol: RNF121
  hgvsc: ENST00000526903.1:n.26+38G>T
  variant of: http://identifiers.org/hgnc/21070
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137522
  ensembl protein: ENSP00000431286
  ensembl transcript: ENST00000530137
  gene symbol: RNF121
  hgvsc: ENST00000530137.1:c.6-3448G>T
  variant of: http://identifiers.org/hgnc/21070
canonical: true
consequence: intron
filter: PASS
num of homozygotes: 1
reference allele: G

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 191
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 921
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3868
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.312335958005249e-4
allele num: 7620
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 1.87133e5

QD
type: SiteQuality
SIO_000300: 1.268e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.72e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.293e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

GenotypeQuality
all individuals: 2344
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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Latino
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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

European (Non-Finnish)
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allele count: 2
allele frequency: 5.165289256198347e-4
allele num: 3872
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 1
allele frequency: 6.281407035175879e-4
allele num: 1592
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.978e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.64e-2

MQRankSum
type: SiteQuality
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DP
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.18e-1

ClippingRankSum
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BaseQRankSum
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SIO_000300: -4.205e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.48e-1

QD
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SIO_000300: 1.491e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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European (Non-Finnish)
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allele count: 2
allele frequency: 5.159958720330237e-4
allele num: 3876
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 198
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 560
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

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

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

QD
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SIO_000300: 1.349e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.77e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.11e-1

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 3.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.86e0

MQRankSum
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SIO_000300: 8.27e-1

DP
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SIO_000300: 1.87135e5

VQSLOD
type: SiteQuality
SIO_000300: 1.4e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 1.312335958005249e-4
allele num: 7620
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3880
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
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SIO_000300: 1.04e1

VQSLOD
type: SiteQuality
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MQRankSum
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.51e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e0

DP
type: SiteQuality
SIO_000300: 1.86754e5

FS
type: SiteQuality
SIO_000300: 4.676e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 6.313131313131314e-4
allele num: 1584
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3866
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 5.434782608695652e-3
allele num: 184
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

Latino
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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
allele num: 7620
num of homozygotes: 0

ReadPosRankSum
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SIO_000300: 6.0e-3

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-1

InbreedingCoeff
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SIO_000300: -2.49e-2

QD
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FS
type: SiteQuality
SIO_000300: 9.34e0

MQRankSum
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DP
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.252e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 64
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GenotypeQuality
all individuals: 27
bin: 8.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1520
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3834
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 198
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.359e1

FS
type: SiteQuality
SIO_000300: 7.785e0

MQRankSum
type: SiteQuality
SIO_000300: 5.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.84e-2

DP
type: SiteQuality
SIO_000300: 1.83769e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.64e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.722e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

VQSLOD
type: SiteQuality
SIO_000300: 3.25e-1

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 23
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3784
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 1.31578947368421e-4
allele num: 7600
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -3.322e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.702e0

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

DP
type: SiteQuality
SIO_000300: 1.79747e5

MQRankSum
type: SiteQuality
SIO_000300: -9.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.12e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.62e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 20
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

European (Finnish)
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allele count: 8
allele frequency: 5.698005698005698e-3
allele num: 1404
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.19e-1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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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

Latino
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allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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Other
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South Asian
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allele frequency: 1.318565400843882e-4
allele num: 7584
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
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QD
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MQ
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FS
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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African
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European (Non-Finnish)
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allele count: 1
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allele num: 3624
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Other
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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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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
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ClippingRankSum
type: SiteQuality
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MQRankSum
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QD
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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South Asian
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allele num: 7420
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European (Non-Finnish)
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European (Finnish)
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Other
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African
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BaseQRankSum
type: SiteQuality
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MQ
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QD
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DP
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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European (Non-Finnish)
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allele num: 3634
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Latino
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Other
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African
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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South Asian
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allele num: 7450
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MQRankSum
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.81e-2

DP
type: SiteQuality
SIO_000300: 1.46158e5

QD
type: SiteQuality
SIO_000300: 1.134e1

FS
type: SiteQuality
SIO_000300: 4.72e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 68
bin: 5.75e1
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GenotypeQuality
all individuals: 61
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3602
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.351351351351351e-4
allele num: 7400
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 910
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.97e-2

QD
type: SiteQuality
SIO_000300: 1.764e1

VQSLOD
type: SiteQuality
SIO_000300: -2.473e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.376e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.45058e5

MQRankSum
type: SiteQuality
SIO_000300: -1.461e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 87
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 348
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 15
allele frequency: 1.969020740351798e-3
allele num: 7618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1588
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3870
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 552
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.32e-2

MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 4.468e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 3.2062e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.86e0

MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.43e-1

QD
type: SiteQuality
SIO_000300: 1.082e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.35e-1

GenotypeQuality
all individuals: 351
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
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GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.625360987135731e-4
allele num: 7618
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 5.494505494505495e-3
allele num: 182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3870
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 43
allele frequency: 7.733812949640288e-2
allele num: 556
num of homozygotes: 4

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.98e-1

QD
type: SiteQuality
SIO_000300: 1.309e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.984e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 2.732e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.22e0

DP
type: SiteQuality
SIO_000300: 3.22917e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

GenotypeQuality
all individuals: 1434
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 379
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4116
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 356
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3874
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 2.624671916010499e-4
allele num: 7620
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: 2.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.397e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.66e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.055e0

DP
type: SiteQuality
SIO_000300: 3.22673e5

QD
type: SiteQuality
SIO_000300: 1.022e1

GenotypeQuality
all individuals: 1484
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 243
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variant carriers: 0

GenotypeQuality
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variant carriers: 4

GenotypeQuality
all individuals: 356
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3874
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 5.249343832020997e-4
allele num: 7620
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.811e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.91e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.83e-2

QD
type: SiteQuality
SIO_000300: 1.266e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

VQSLOD
type: SiteQuality
SIO_000300: -2.212e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.3e-1

DP
type: SiteQuality
SIO_000300: 3.22976e5

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 357
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 222
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variant carriers: 0

GenotypeQuality
all individuals: 4116
bin: 9.75e1
variant carriers: 5

Latino
type: Population
allele count: 1
allele frequency: 5.376344086021506e-3
allele num: 186
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3872
num of homozygotes: 0

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

African
type: Population
allele count: 4
allele frequency: 7.168458781362007e-3
allele num: 558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.912e1

DP
type: SiteQuality
SIO_000300: 3.22703e5

BaseQRankSum
type: SiteQuality
SIO_000300: 4.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.71e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.14e-1

FS
type: SiteQuality
SIO_000300: 4.372e0

QD
type: SiteQuality
SIO_000300: 1.535e1

VQSLOD
type: SiteQuality
SIO_000300: -2.214e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 32
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 7
allele frequency: 9.861932938856016e-4
allele num: 7098
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 90
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2476
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.48e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.05e-2

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.493e0

DP
type: SiteQuality
SIO_000300: 1.17371e5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 16
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2652
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.339405304045004e-4
allele num: 7466
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 92
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East Asian
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allele frequency: 0.0e0
allele num: 132
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MQ
type: SiteQuality
SIO_000300: 4.759e1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -4.827e-1

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.359e0

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.76e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.35286e5

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 132
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South Asian
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allele frequency: 3.996802557953637e-4
allele num: 7506
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 1.08695652173913e-2
allele num: 92
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 1.694915254237288e-2
allele num: 118
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.225e0

MQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

MQ
type: SiteQuality
SIO_000300: 5.942e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.21e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.154e-1

QD
type: SiteQuality
SIO_000300: 1.569e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.03e0

DP
type: SiteQuality
SIO_000300: 1.36945e5

ClippingRankSum
type: SiteQuality
SIO_000300: -5.16e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 1.332267519317879e-4
allele num: 7506
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 2722
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East Asian
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 2.872e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e-2

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.372e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.38e-1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.12e-2

DP
type: SiteQuality
SIO_000300: 1.36245e5

QD
type: SiteQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 90
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African
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allele count: 3
allele frequency: 1.595744680851064e-2
allele num: 188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

DP
type: SiteQuality
SIO_000300: 1.16869e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-1

BaseQRankSum
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.26e-1

FS
type: SiteQuality
SIO_000300: 1.3732e1

VQSLOD
type: SiteQuality
SIO_000300: -5.316e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.44e-2

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 88
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2588
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.14859e5

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-2

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.04e-2

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.062e0

East Asian
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allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 88
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South Asian
type: Population
allele count: 1
allele frequency: 1.38121546961326e-4
allele num: 7240
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.767e0

VQSLOD
type: SiteQuality
SIO_000300: -1.948e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.56e-1

DP
type: SiteQuality
SIO_000300: 1.15016e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
type: SiteQuality
SIO_000300: -3.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.01e-2

QD
type: SiteQuality
SIO_000300: 1.23e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2740
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.267e0

MQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.44982e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.21e-2

QD
type: SiteQuality
SIO_000300: 1.992e1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8710
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.77e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.44844e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

QD
type: SiteQuality
SIO_000300: 1.275e1

MQ
type: SiteQuality
SIO_000300: 5.604e1

VQSLOD
type: SiteQuality
SIO_000300: 7.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

South Asian
type: Population
allele count: 2
allele frequency: 2.538715410002539e-4
allele num: 7878
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 19
allele frequency: 2.181901699586587e-3
allele num: 8708
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2740
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.37e1

MQRankSum
type: SiteQuality
SIO_000300: 4.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.187e0

MQ
type: SiteQuality
SIO_000300: 5.89e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.049999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.93e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 5.45313e5

East Asian
type: Population
allele count: 18
allele frequency: 2.821316614420063e-2
allele num: 638
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 1.822157434402332e-3
allele num: 2744
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30
num of homozygotes: 0

South Asian
type: Population
allele count: 91
allele frequency: 1.155408836973083e-2
allele num: 7876
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 155
allele frequency: 1.778746844158825e-2
allele num: 8714
num of homozygotes: 1

Latino
type: Population
allele count: 10
allele frequency: 2.5e-2
allele num: 400
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.92e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.517e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.91e-2

QD
type: SiteQuality
SIO_000300: 1.416e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.41e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 5.47297e5

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.35e0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8714
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 638
num of homozygotes: 0

African
type: Population
allele count: 20
allele frequency: 7.293946024799417e-3
allele num: 2742
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7872
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e-1

DP
type: SiteQuality
SIO_000300: 5.46356e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.88e-2

MQ
type: SiteQuality
SIO_000300: 5.911e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.45e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.7e-1

GenotypeQuality
all individuals: 840
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 503
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.269680040629761e-4
allele num: 7876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 648
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8790
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.886e1

VQSLOD
type: SiteQuality
SIO_000300: -8.991e-1

QD
type: SiteQuality
SIO_000300: 6.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.034e0

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.610000000000001e-2

DP
type: SiteQuality
SIO_000300: 5.5644e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.1e-2

GenotypeQuality
all individuals: 1284
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 445
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variant carriers: 0

GenotypeQuality
all individuals: 347
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variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 242
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52114390021296e-4
allele num: 6574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2274
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 142
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.915e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.619999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.1e-2

QD
type: SiteQuality
SIO_000300: 6.08e0

FS
type: SiteQuality
SIO_000300: 3.3167e1

MQRankSum
type: SiteQuality
SIO_000300: 9.389999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.13e0

DP
type: SiteQuality
SIO_000300: 5.92309e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.98e0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4485
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 744
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8834
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 2.150537634408602e-3
allele num: 2790
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7884
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.74e0

MQ
type: SiteQuality
SIO_000300: 5.944e1

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

DP
type: SiteQuality
SIO_000300: 6.11793e5

VQSLOD
type: SiteQuality
SIO_000300: -7.733e-1

FS
type: SiteQuality
SIO_000300: 4.422e0

QD
type: SiteQuality
SIO_000300: 1.53e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.84e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.95e-1

GenotypeQuality
all individuals: 1002
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1191
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 102
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1878
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.949317738791423e-4
allele num: 5130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4704
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.994e0

MQ
type: SiteQuality
SIO_000300: 5.876e1

QD
type: SiteQuality
SIO_000300: 6.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-1

DP
type: SiteQuality
SIO_000300: 6.16343e5

VQSLOD
type: SiteQuality
SIO_000300: -7.115000000000001e1

FS
type: SiteQuality
SIO_000300: 1.27751e2

MQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.169e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.061e0

GenotypeQuality
all individuals: 160
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 8

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
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GenotypeQuality
all individuals: 161
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variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 2.031340684852002e-3
allele num: 3446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 72
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 6.180469715698393e-4
allele num: 3236
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 5.966587112171838e-4
allele num: 1676
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 262
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.442e0

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-1

QD
type: SiteQuality
SIO_000300: 6.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.309e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.366e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.388e0

DP
type: SiteQuality
SIO_000300: 6.73668e5

FS
type: SiteQuality
SIO_000300: 2.38259e2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.09e0

MQ
type: SiteQuality
SIO_000300: 5.863e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 379
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.25e1
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GenotypeQuality
all individuals: 382
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.506024096385542e-3
allele num: 664
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7884
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 7.65613e5

MQRankSum
type: SiteQuality
SIO_000300: 2.88e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.251e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.79e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.574e0

FS
type: SiteQuality
SIO_000300: 2.452e0

MQ
type: SiteQuality
SIO_000300: 5.897e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

QD
type: SiteQuality
SIO_000300: 7.58e0

GenotypeQuality
all individuals: 375
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 253
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
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variant carriers: 0

GenotypeQuality
all individuals: 16918
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GenotypeQuality
all individuals: 113
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GenotypeQuality
all individuals: 121
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GenotypeQuality
all individuals: 163
bin: 3.75e1
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GenotypeQuality
all individuals: 148
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GenotypeQuality
all individuals: 47
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GenotypeQuality
all individuals: 87
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GenotypeQuality
all individuals: 62
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GenotypeQuality
all individuals: 180
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 261
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.572327044025157e-3
allele num: 1272
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 1.631321370309951e-3
allele num: 2452
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.380952380952381e-2
allele num: 42
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 4.364694471387003e-3
allele num: 2062
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.379e2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.855e0

MQRankSum
type: SiteQuality
SIO_000300: 2.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.054e-1

MQ
type: SiteQuality
SIO_000300: 5.883e1

FS
type: SiteQuality
SIO_000300: 2.68948e2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.478e0

DP
type: SiteQuality
SIO_000300: 7.47601e5

QD
type: SiteQuality
SIO_000300: 3.85e0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4
allele frequency: 1.834862385321101e-2
allele num: 218
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2062
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1272
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2452
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.054e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.49e0

MQ
type: SiteQuality
SIO_000300: 5.883e1

MQRankSum
type: SiteQuality
SIO_000300: 2.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.478e0

FS
type: SiteQuality
SIO_000300: 2.68948e2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.855e0

QD
type: SiteQuality
SIO_000300: 3.85e0

VQSLOD
type: SiteQuality
SIO_000300: -3.379e2

DP
type: SiteQuality
SIO_000300: 7.47601e5

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

African
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allele count: 1
allele frequency: 3.558718861209965e-4
allele num: 2810
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.25123818099955e-4
allele num: 8884
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7846
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.236e0

FS
type: SiteQuality
SIO_000300: 1.7637e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.28e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.564e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.13e-1

QD
type: SiteQuality
SIO_000300: 1.165e1

MQ
type: SiteQuality
SIO_000300: 5.895e1

DP
type: SiteQuality
SIO_000300: 6.61707e5

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.768e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

African
type: Population
allele count: 1
allele frequency: 3.563791874554526e-4
allele num: 2806
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.124606387764283e-4
allele num: 8892
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

DP
type: SiteQuality
SIO_000300: 6.64125e5

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.415e1

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.687e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 27
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GenotypeQuality
all individuals: 171
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2806
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 660
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.12637981527371e-4
allele num: 8878
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.66282e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.183e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.43e-2

FS
type: SiteQuality
SIO_000300: 1.047e0

MQRankSum
type: SiteQuality
SIO_000300: 2.94e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.695e0

QD
type: SiteQuality
SIO_000300: 1.185e1

VQSLOD
type: SiteQuality
SIO_000300: 2.4e-1

MQ
type: SiteQuality
SIO_000300: 5.658e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3813
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2818
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8876
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.288992008249549e-4
allele num: 7758
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.917e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e-1

VQSLOD
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ClippingRankSum
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SIO_000300: -8.2e-2

FS
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SIO_000300: 4.179e0

DP
type: SiteQuality
SIO_000300: 6.73383e5

InbreedingCoeff
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SIO_000300: -7.46e-2

BaseQRankSum
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SIO_000300: 1.33e0

MQRankSum
type: SiteQuality
SIO_000300: 6.23e-1

QD
type: SiteQuality
SIO_000300: 1.262e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8880
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 2824
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.584647195657793e-4
allele num: 7738
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.58e-1

MQRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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MQ
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BaseQRankSum
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QD
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ReadPosRankSum
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DP
type: SiteQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.128923007450892e-4
allele num: 8858
num of homozygotes: 0

South Asian
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allele count: 0
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allele num: 7630
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 418
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 2826
num of homozygotes: 0

Other
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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

FS
type: SiteQuality
SIO_000300: 3.77e0

InbreedingCoeff
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DP
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QD
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MQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.129943502824859e-4
allele num: 8850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 46
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2826
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.857e0

VQSLOD
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SIO_000300: -2.819e0

DP
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SIO_000300: 6.73689e5

MQ
type: SiteQuality
SIO_000300: 5.92e1

BaseQRankSum
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SIO_000300: -2.327e0

InbreedingCoeff
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SIO_000300: -7.41e-2

MQRankSum
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SIO_000300: -1.13e0

FS
type: SiteQuality
SIO_000300: 2.858e0

QD
type: SiteQuality
SIO_000300: 9.68e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8832
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.328374070138151e-4
allele num: 7528
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2822
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.69677e5

ClippingRankSum
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SIO_000300: 7.73e-1

MQ
type: SiteQuality
SIO_000300: 5.815e1

VQSLOD
type: SiteQuality
SIO_000300: -1.938e0

InbreedingCoeff
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SIO_000300: -7.480000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 2.54e0

MQRankSum
type: SiteQuality
SIO_000300: 9.99e-1

QD
type: SiteQuality
SIO_000300: 1.286e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3859
bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8748
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7326
num of homozygotes: 0

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

African
type: Population
allele count: 5
allele frequency: 1.77683013503909e-3
allele num: 2814
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.57376e5

BaseQRankSum
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SIO_000300: 7.27e-1

ClippingRankSum
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SIO_000300: 3.58e-1

InbreedingCoeff
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SIO_000300: -7.51e-2

QD
type: SiteQuality
SIO_000300: 1.362e1

VQSLOD
type: SiteQuality
SIO_000300: 2.56e0

FS
type: SiteQuality
SIO_000300: 1.105e0

MQRankSum
type: SiteQuality
SIO_000300: 1.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.84e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8706
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.558718861209965e-4
allele num: 2810
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.833e1

MQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.38e-1

BaseQRankSum
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SIO_000300: 4.1e0

FS
type: SiteQuality
SIO_000300: 5.82e-1

InbreedingCoeff
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SIO_000300: -7.65e-2

VQSLOD
type: SiteQuality
SIO_000300: -8.829e-1

DP
type: SiteQuality
SIO_000300: 6.4836e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.34e-1

QD
type: SiteQuality
SIO_000300: 1.221e1

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1717
bin: 6.25e1
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GenotypeQuality
all individuals: 128
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.568879371877231e-4
allele num: 2802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6820
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

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

InbreedingCoeff
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ClippingRankSum
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SIO_000300: -1.005e0

VQSLOD
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FS
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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DP
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SIO_000300: 6.14966e5

MQ
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SIO_000300: 5.687e1

QD
type: SiteQuality
SIO_000300: 9.42e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
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

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

Latino
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allele frequency: 0.0e0
allele num: 406
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6720
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.87e-1

FS
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SIO_000300: 0.0e0

InbreedingCoeff
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MQ
type: SiteQuality
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DP
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SIO_000300: 6.09026e5

QD
type: SiteQuality
SIO_000300: 1.2e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5712
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
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

European (Finnish)
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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

Latino
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allele frequency: 2.577319587628866e-3
allele num: 388
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.895e0

MQRankSum
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QD
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FS
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DP
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MQ
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -7.2e-1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4015
bin: 7.25e1
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GenotypeQuality
all individuals: 3134
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.646922631680494e-5
allele num: 10366
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66518
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.127e1

VQSLOD
type: SiteQuality
SIO_000300: -2.822e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.14e0

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 4.132083e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQ
type: SiteQuality
SIO_000300: 5.86e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.24e0

GenotypeDepth
all individuals: 5792
bin: 6.75e1
variant carriers: 23

GenotypeDepth
all individuals: 4418
bin: 7.25e1
variant carriers: 24

GenotypeQuality
all individuals: 193
bin: 7.5e0
variant carriers: 5

GenotypeQuality
all individuals: 1046
bin: 9.25e1
variant carriers: 8

GenotypeQuality
all individuals: 250
bin: 3.75e1
variant carriers: 17

GenotypeQuality
all individuals: 248
bin: 2.25e1
variant carriers: 12

GenotypeQuality
all individuals: 12284
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variant carriers: 15

GenotypeQuality
all individuals: 2924
bin: 8.25e1
variant carriers: 12

GenotypeQuality
all individuals: 244
bin: 3.25e1
variant carriers: 25

GenotypeQuality
all individuals: 4997
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GenotypeQuality
all individuals: 176
bin: 1.25e1
variant carriers: 13

GenotypeQuality
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GenotypeQuality
all individuals: 263
bin: 4.25e1
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GenotypeQuality
all individuals: 24756
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variant carriers: 13

GenotypeQuality
all individuals: 3885
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variant carriers: 18

GenotypeQuality
all individuals: 302
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variant carriers: 13

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 163
bin: 1.75e1
variant carriers: 11

GenotypeQuality
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bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 954
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variant carriers: 10

GenotypeQuality
all individuals: 3097
bin: 9.75e1
variant carriers: 341

GenotypeQuality
all individuals: 202
bin: 2.75e1
variant carriers: 14

European (Non-Finnish)
type: Population
allele count: 282
allele frequency: 4.604833442194644e-3
allele num: 61240
num of homozygotes: 0

African
type: Population
allele count: 77
allele frequency: 8.582255907267054e-3
allele num: 8972
num of homozygotes: 0

East Asian
type: Population
allele count: 62
allele frequency: 7.473481195756991e-3
allele num: 8296
num of homozygotes: 0

South Asian
type: Population
allele count: 13
allele frequency: 7.927796072691791e-4
allele num: 16398
num of homozygotes: 0

Latino
type: Population
allele count: 14
allele frequency: 1.26012601260126e-3
allele num: 11110
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 7.594936708860759e-3
allele num: 790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 84
allele frequency: 1.588502269288956e-2
allele num: 5288
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.978e1

MQ
type: SiteQuality
SIO_000300: 5.908e1

FS
type: SiteQuality
SIO_000300: 1.46334e2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.69e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.78e0

DP
type: SiteQuality
SIO_000300: 3.872522e6

QD
type: SiteQuality
SIO_000300: 2.38e0

MQRankSum
type: SiteQuality
SIO_000300: -1.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.189e0

GenotypeDepth
all individuals: 837
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5826
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variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 64
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GenotypeQuality
all individuals: 74
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3390
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GenotypeQuality
all individuals: 74
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GenotypeQuality
all individuals: 48
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GenotypeQuality
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GenotypeQuality
all individuals: 118
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GenotypeQuality
all individuals: 205
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GenotypeQuality
all individuals: 26743
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GenotypeQuality
all individuals: 193
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GenotypeQuality
all individuals: 1116
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GenotypeQuality
all individuals: 1255
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variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3304
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507704369327262e-5
allele num: 66326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.087e1

MQ
type: SiteQuality
SIO_000300: 5.805e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.329e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

QD
type: SiteQuality
SIO_000300: 5.06e0

FS
type: SiteQuality
SIO_000300: 1.01816e2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e0

MQRankSum
type: SiteQuality
SIO_000300: 2.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.495e0

DP
type: SiteQuality
SIO_000300: 3.86417e6

GenotypeDepth
all individuals: 1456
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2627
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variant carriers: 1

GenotypeQuality
all individuals: 27146
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
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GenotypeQuality
all individuals: 1105
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GenotypeQuality
all individuals: 13502
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variant carriers: 0

GenotypeQuality
all individuals: 56
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GenotypeQuality
all individuals: 150
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variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 3344
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variant carriers: 1

GenotypeQuality
all individuals: 211
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GenotypeQuality
all individuals: 84
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GenotypeQuality
all individuals: 3313
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variant carriers: 0

GenotypeQuality
all individuals: 89
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variant carriers: 0

GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 73
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GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 5613
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4297
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GenotypeQuality
all individuals: 1246
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variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 89
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.658103148541626e-5
allele num: 10354
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.54273372415921e-4
allele num: 6482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66462
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.02e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.73e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.941e0

QD
type: SiteQuality
SIO_000300: 1.44e0

DP
type: SiteQuality
SIO_000300: 3.866216e6

MQRankSum
type: SiteQuality
SIO_000300: -1.89e-1

FS
type: SiteQuality
SIO_000300: 3.0291e1

MQ
type: SiteQuality
SIO_000300: 5.871e1

GenotypeDepth
all individuals: 1044
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5840
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
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variant carriers: 0

GenotypeQuality
all individuals: 3325
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 13581
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variant carriers: 0

GenotypeQuality
all individuals: 200
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 7
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GenotypeQuality
all individuals: 111
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GenotypeQuality
all individuals: 1248
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variant carriers: 0

GenotypeQuality
all individuals: 38
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GenotypeQuality
all individuals: 5636
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 1108
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variant carriers: 0

GenotypeQuality
all individuals: 4314
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variant carriers: 0

GenotypeQuality
all individuals: 76
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GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 52
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GenotypeQuality
all individuals: 3421
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 7.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 2.844e0

VQSLOD
type: SiteQuality
SIO_000300: 7.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e-1

QD
type: SiteQuality
SIO_000300: 1.069e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.781e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

DP
type: SiteQuality
SIO_000300: 3.870196e6

GenotypeDepth
all individuals: 1459
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7119
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variant carriers: 0

GenotypeQuality
all individuals: 13568
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GenotypeQuality
all individuals: 3306
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GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 88
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GenotypeQuality
all individuals: 47
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GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 55
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GenotypeQuality
all individuals: 4305
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variant carriers: 0

GenotypeQuality
all individuals: 53
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GenotypeQuality
all individuals: 204
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GenotypeQuality
all individuals: 82
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GenotypeQuality
all individuals: 16
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GenotypeQuality
all individuals: 1243
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GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1100
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GenotypeQuality
all individuals: 33
bin: 4.25e1
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GenotypeQuality
all individuals: 3293
bin: 9.75e1
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GenotypeQuality
all individuals: 5626
bin: 7.75e1
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GenotypeQuality
all individuals: 27521
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.676036786395974e-5
allele num: 11526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66488
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.544163063619518e-4
allele num: 6476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.643201542912247e-5
allele num: 10370
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

ClippingRankSum
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SIO_000300: -1.532e0

VQSLOD
type: SiteQuality
SIO_000300: -6.187e0

FS
type: SiteQuality
SIO_000300: 3.392e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.621e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 3.87098e6

GenotypeDepth
all individuals: 1461
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 7056
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3292
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variant carriers: 3

GenotypeQuality
all individuals: 4311
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GenotypeQuality
all individuals: 2
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variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e0

FS
type: SiteQuality
SIO_000300: 4.063e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.163e0

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

MQRankSum
type: SiteQuality
SIO_000300: 3.26e-1

QD
type: SiteQuality
SIO_000300: 1.348e1

DP
type: SiteQuality
SIO_000300: 3.878976e6

GenotypeDepth
all individuals: 4476
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variant carriers: 0

GenotypeDepth
all individuals: 4007
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 13699
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GenotypeQuality
all individuals: 28077
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GenotypeQuality
all individuals: 3313
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 4311
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10404
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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: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

VQSLOD
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ClippingRankSum
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FS
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InbreedingCoeff
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QD
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MQ
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BaseQRankSum
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DP
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SIO_000300: 3.878976e6

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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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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Other
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ClippingRankSum
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DP
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MQRankSum
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QD
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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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InbreedingCoeff
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SIO_000300: 0.0e0

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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bin: 7.25e1
variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
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 frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

MQRankSum
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ReadPosRankSum
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FS
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QD
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DP
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VQSLOD
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SIO_000300: 1.13e0

InbreedingCoeff
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ClippingRankSum
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SIO_000300: -1.51e-1

BaseQRankSum
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SIO_000300: 7.11e-1

MQ
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SIO_000300: 5.967e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 31

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 35

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

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

East Asian
type: Population
allele count: 35
allele frequency: 4.044372544488098e-3
allele num: 8654
num of homozygotes: 1

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

MQRankSum
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SIO_000300: -5.5e-2

FS
type: SiteQuality
SIO_000300: 5.17e-1

QD
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SIO_000300: 1.173e1

ReadPosRankSum
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SIO_000300: -2.86e-1

InbreedingCoeff
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SIO_000300: 3.71e-2

MQ
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SIO_000300: 5.969e1

BaseQRankSum
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SIO_000300: -2.662e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.06e-1

DP
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SIO_000300: 3.88119e6

GenotypeDepth
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variant carriers: 56

GenotypeDepth
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variant carriers: 36

GenotypeDepth
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variant carriers: 50

GenotypeDepth
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variant carriers: 20

GenotypeDepth
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variant carriers: 867

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 112
allele frequency: 6.782945736434108e-3
allele num: 16512
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 906
allele frequency: 1.357791565506699e-2
allele num: 66726
num of homozygotes: 4

African
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allele count: 27
allele frequency: 2.59515570934256e-3
allele num: 10404
num of homozygotes: 1

European (Finnish)
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allele count: 38
allele frequency: 5.745388569700635e-3
allele num: 6614
num of homozygotes: 2

Latino
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allele count: 60
allele frequency: 5.182242183451373e-3
allele num: 11578
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 13
allele frequency: 1.431718061674009e-2
allele num: 908
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MQ
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SIO_000300: 5.989e1

InbreedingCoeff
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FS
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SIO_000300: 5.41e-1

ReadPosRankSum
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MQRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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SIO_000300: -7.16e-1

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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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: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

East Asian
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European (Finnish)
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Other
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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MQRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 6.023e1

FS
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DP
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SIO_000300: 3.888846e6

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

South Asian
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allele 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

European (Finnish)
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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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DP
type: SiteQuality
SIO_000300: 3.888748e6

MQRankSum
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QD
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SIO_000300: 1.32e1

VQSLOD
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BaseQRankSum
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SIO_000300: -2.281e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.858e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.45e-1

InbreedingCoeff
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SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 36

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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variant carriers: 59

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 4367
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variant carriers: 0

Latino
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allele count: 3
allele frequency: 2.591568762957844e-4
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 40
allele frequency: 5.994664748373948e-4
allele num: 66726
num of homozygotes: 0

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

African
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allele count: 3
allele frequency: 2.883506343713956e-4
allele num: 10404
num of homozygotes: 0

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

South Asian
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allele count: 14
allele frequency: 8.478682170542636e-4
allele num: 16512
num of homozygotes: 1

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.79e-1

QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.92e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.216e0

DP
type: SiteQuality
SIO_000300: 3.891149e6

MQRankSum
type: SiteQuality
SIO_000300: 2.26e-1

FS
type: SiteQuality
SIO_000300: 1.261e0

MQ
type: SiteQuality
SIO_000300: 6.014e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e-1

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
all individuals: 28634
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.373e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.376e0

MQRankSum
type: SiteQuality
SIO_000300: -7.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.79e-1

QD
type: SiteQuality
SIO_000300: 2.007e1

VQSLOD
type: SiteQuality
SIO_000300: -5.033e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.9e-2

MQ
type: SiteQuality
SIO_000300: 5.975e1

DP
type: SiteQuality
SIO_000300: 3.888939e6

GenotypeDepth
all individuals: 2572
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variant carriers: 2

GenotypeDepth
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variant carriers: 4

GenotypeDepth
all individuals: 1510
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variant carriers: 6

GenotypeDepth
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 114

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4368
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GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 109
allele frequency: 1.047673971549404e-2
allele num: 10404
num of homozygotes: 1

Latino
type: Population
allele count: 5
allele frequency: 4.320027648176948e-4
allele num: 11574
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.892631e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.78e-1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

FS
type: SiteQuality
SIO_000300: 6.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.17e-1

QD
type: SiteQuality
SIO_000300: 1.421e1

MQ
type: SiteQuality
SIO_000300: 5.995e1

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 12

GenotypeQuality
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GenotypeQuality
all individuals: 17
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

South Asian
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allele count: 11
allele frequency: 6.663435909861885e-4
allele num: 16508
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QD
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BaseQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 4.74e-1

InbreedingCoeff
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SIO_000300: 2.02e-2

ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.52e-1

DP
type: SiteQuality
SIO_000300: 3.887703e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 710
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variant carriers: 0

GenotypeQuality
all individuals: 49
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GenotypeQuality
all individuals: 115
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GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2112
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
all individuals: 5571
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GenotypeQuality
all individuals: 1083
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variant carriers: 0

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

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele count: 7
allele frequency: 6.058507876060239e-4
allele num: 11554
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.91e0

FS
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.035e1

ClippingRankSum
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VQSLOD
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QD
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DP
type: SiteQuality
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