11-562262-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562262
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562262
    reference: chr 11
allele count: 1
allele frequency: 8.424741781664392e-6
allele num: 118698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.308C>T
  hgvsp: ENSP00000405606.2:p.Pro103Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.308C>T
  hgvsp: ENSP00000380712.3:p.Pro103Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.231C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.308C>T
  hgvsp: ENSP00000403068.1:p.Pro103Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.308C>T
  hgvsp: ENSP00000380713.3:p.Pro103Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.303C>T
  hgvsp: ENST00000414138.2:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.308C>T
  hgvsp: ENSP00000344226.4:p.Pro103Leu
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1488
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50158
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro103Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-562263-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562263
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562263
    reference: chr 11
allele count: 4
allele frequency: 3.369385760975774e-5
allele num: 118716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.309G>A
  hgvsp: ENST00000344375.4:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.304G>A
  hgvsp: ENSP00000413484.2:p.Gly102Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.309G>A
  hgvsp: ENST00000454668.2:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.309G>A
  hgvsp: ENST00000431809.1:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.309G>A
  hgvsp: ENST00000397582.3:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.309G>A
  hgvsp: ENST00000397583.3:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.232G>A
  variant of: http://identifiers.org/hgnc/1166
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5157
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly102Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-562266-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562266
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562266
    reference: chr 11
allele count: 1
allele frequency: 8.430992327796981e-6
allele num: 118610
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.312A>C
  hgvsp: ENSP00000380713.3:p.Glu104Asp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.312A>C
  hgvsp: ENSP00000403068.1:p.Glu104Asp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.312A>C
  hgvsp: ENSP00000344226.4:p.Glu104Asp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.312A>C
  hgvsp: ENSP00000405606.2:p.Glu104Asp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.307A>C
  hgvsp: ENSP00000413484.2:p.Thr103Pro
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.312A>C
  hgvsp: ENSP00000380712.3:p.Glu104Asp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.235A>C
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu104Asp
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: A
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP

11-562267-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562267
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562267
    reference: chr 11
allele count: 3
allele frequency: 2.52925505007925e-5
allele num: 118612
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.313C>T
  hgvsp: ENSP00000380713.3:p.Arg105Cys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.313C>T
  hgvsp: ENSP00000380712.3:p.Arg105Cys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.308C>T
  hgvsp: ENSP00000413484.2:p.Thr103Met
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.313C>T
  hgvsp: ENSP00000403068.1:p.Arg105Cys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.313C>T
  hgvsp: ENSP00000344226.4:p.Arg105Cys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.313C>T
  hgvsp: ENSP00000405606.2:p.Arg105Cys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.236C>T
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3835
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg105Cys
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD

11-562268-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562268
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562268
    reference: chr 11
allele count: 3
allele frequency: 2.530449745268059e-5
allele num: 118556
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.314G>A
  hgvsp: ENSP00000344226.4:p.Arg105His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.314G>A
  hgvsp: ENSP00000405606.2:p.Arg105His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.309G>A
  hgvsp: ENST00000414138.2:c.309G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.314G>A
  hgvsp: ENSP00000403068.1:p.Arg105His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.237G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.314G>A
  hgvsp: ENSP00000380712.3:p.Arg105His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.314G>A
  hgvsp: ENSP00000380713.3:p.Arg105His
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50135
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg105His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

11-562269-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562269
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562269
    reference: chr 11
allele count: 1
allele frequency: 8.445375312478886e-6
allele num: 118408
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.238C>G
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.315C>G
  hgvsp: ENST00000344375.4:c.315C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.315C>G
  hgvsp: ENST00000431809.1:c.315C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.315C>G
  hgvsp: ENST00000397583.3:c.315C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.315C>G
  hgvsp: ENST00000397582.3:c.315C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.310C>G
  hgvsp: ENSP00000413484.2:p.Leu104Val
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.315C>G
  hgvsp: ENST00000454668.2:c.315C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16747
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49874
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1775
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu104Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS

11-562279-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562279
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562279
    reference: chr 11
allele count: 1
allele frequency: 8.494588946840863e-6
allele num: 117722
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.325C>G
  hgvsp: ENSP00000344226.4:p.Arg109Gly
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.320C>G
  hgvsp: ENSP00000413484.2:p.Ser107Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.325C>G
  hgvsp: ENSP00000380712.3:p.Arg109Gly
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.248C>G
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.325C>G
  hgvsp: ENSP00000380713.3:p.Arg109Gly
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.325C>G
  hgvsp: ENSP00000403068.1:p.Arg109Gly
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.325C>G
  hgvsp: ENSP00000405606.2:p.Arg109Gly
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16412
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 965
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg109Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-562280-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562280
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562280
    reference: chr 11
allele count: 8
allele frequency: 6.802258349772124e-5
allele num: 117608
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.326G>A
  hgvsp: ENSP00000380712.3:p.Arg109His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.249G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.326G>A
  hgvsp: ENSP00000405606.2:p.Arg109His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.326G>A
  hgvsp: ENSP00000380713.3:p.Arg109His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.321G>A
  hgvsp: ENST00000414138.2:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.326G>A
  hgvsp: ENSP00000344226.4:p.Arg109His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.326G>A
  hgvsp: ENSP00000403068.1:p.Arg109His
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 342
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2460
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg109His
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

11-562286-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562286
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562286
    reference: chr 11
allele count: 2
allele frequency: 1.709314052270824e-5
allele num: 117006
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.332G>A
  hgvsp: ENSP00000380712.3:p.Ser111Asn
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.332G>A
  hgvsp: ENSP00000380713.3:p.Ser111Asn
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.332G>A
  hgvsp: ENSP00000403068.1:p.Ser111Asn
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.332G>A
  hgvsp: ENSP00000344226.4:p.Ser111Asn
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.327G>A
  hgvsp: ENST00000414138.2:c.327G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.255G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.332G>A
  hgvsp: ENSP00000405606.2:p.Ser111Asn
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48245
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4944
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser111Asn
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-562293-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562293
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562293
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 115666
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.339T>C
  hgvsp: ENST00000397582.3:c.339T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.339T>C
  hgvsp: ENST00000454668.2:c.339T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.262T>C
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.334T>C
  hgvsp: ENSP00000413484.2:p.Cys112Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.339T>C
  hgvsp: ENST00000397583.3:c.339T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.339T>C
  hgvsp: ENST00000431809.1:c.339T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.339T>C
  hgvsp: ENST00000344375.4:c.339T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33747
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4748
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4494
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Cys112Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

11-562298-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562298
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562298
    reference: chr 11
allele count: 1
allele frequency: 8.773007211411927e-6
allele num: 113986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.344A>T
  hgvsp: ENSP00000405606.2:p.Lys115Met
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.344A>T
  hgvsp: ENSP00000344226.4:p.Lys115Met
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.267A>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.344A>T
  hgvsp: ENSP00000380713.3:p.Lys115Met
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.339A>T
  hgvsp: ENSP00000413484.2:p.Lys113Asn
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.344A>T
  hgvsp: ENSP00000403068.1:p.Lys115Met
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.344A>T
  hgvsp: ENSP00000380712.3:p.Lys115Met
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4550
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15119
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6361
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys115Met
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

11-562299-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562299
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562299
    reference: chr 11
allele count: 1
allele frequency: 8.912179384346648e-6
allele num: 112206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.345G>A
  hgvsp: ENST00000344375.4:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.345G>A
  hgvsp: ENST00000397582.3:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.268G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.345G>A
  hgvsp: ENST00000454668.2:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.345G>A
  hgvsp: ENST00000431809.1:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.340G>A
  hgvsp: ENSP00000413484.2:p.Ala114Thr
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.345G>A
  hgvsp: ENST00000397583.3:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14198
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4094
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8265
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala114Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

11-562301-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562301
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562301
    reference: chr 11
allele count: 1
allele frequency: 8.915993509156726e-6
allele num: 112158
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.347C>G
  hgvsp: ENSP00000405606.2:p.Pro116Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.347C>G
  hgvsp: ENSP00000403068.1:p.Pro116Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.347C>G
  hgvsp: ENSP00000380713.3:p.Pro116Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.347C>G
  hgvsp: ENSP00000380712.3:p.Pro116Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.347C>G
  hgvsp: ENSP00000344226.4:p.Pro116Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.342C>G
  hgvsp: ENST00000414138.2:c.342C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.270C>G
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3262
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30326
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1047
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4090
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1169
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro116Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

11-562301-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562301
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562301
    reference: chr 11
allele count: 1
allele frequency: 8.915993509156726e-6
allele num: 112158
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.347C>T
  hgvsp: ENSP00000344226.4:p.Pro116Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.347C>T
  hgvsp: ENSP00000380713.3:p.Pro116Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.270C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.347C>T
  hgvsp: ENSP00000380712.3:p.Pro116Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.347C>T
  hgvsp: ENSP00000403068.1:p.Pro116Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.342C>T
  hgvsp: ENST00000414138.2:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.347C>T
  hgvsp: ENSP00000405606.2:p.Pro116Leu
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30326
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1169
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro116Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-562302-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562302
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562302
    reference: chr 11
allele count: 1
allele frequency: 8.950147677436678e-6
allele num: 111730
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.348A>G
  hgvsp: ENST00000431809.1:c.348A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.271A>G
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.348A>G
  hgvsp: ENST00000397582.3:c.348A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.343A>G
  hgvsp: ENSP00000413484.2:p.Thr115Ala
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.348A>G
  hgvsp: ENST00000454668.2:c.348A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.348A>G
  hgvsp: ENST00000397583.3:c.348A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.348A>G
  hgvsp: ENST00000344375.4:c.348A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6568
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3965
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14014
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40911
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr115Ala
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum

11-562303-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562303
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562303
    reference: chr 11
allele count: 7
allele frequency: 6.290890790135883e-5
allele num: 111272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.349C>T
  hgvsp: ENSP00000403068.1:p.Arg117Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.349C>T
  hgvsp: ENSP00000405606.2:p.Arg117Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.349C>T
  hgvsp: ENSP00000344226.4:p.Arg117Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.349C>T
  hgvsp: ENSP00000380712.3:p.Arg117Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.349C>T
  hgvsp: ENSP00000380713.3:p.Arg117Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.344C>T
  hgvsp: ENSP00000413484.2:p.Thr115Met
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.272C>T
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6972
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3143
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13767
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40296
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 791
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg117Trp
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

11-562304-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562304
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562304
    reference: chr 11
allele count: 2
allele frequency: 1.850275691077971e-5
allele num: 108092
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.350G>A
  hgvsp: ENSP00000380713.3:p.Arg117Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.273G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.350G>A
  hgvsp: ENSP00000405606.2:p.Arg117Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.350G>A
  hgvsp: ENSP00000380712.3:p.Arg117Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.345G>A
  hgvsp: ENST00000414138.2:c.345G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.350G>A
  hgvsp: ENSP00000344226.4:p.Arg117Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.350G>A
  hgvsp: ENSP00000403068.1:p.Arg117Gln
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12225
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1292
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1762
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12879
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Arg117Gln
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

11-562305-GGCTGCGCTGGGCTGTGAGCCCCGC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562305
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562281
    reference: chr 11
allele count: 3
allele frequency: 2.774540813495367e-5
allele num: 108126
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: coding_sequence_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsp: ENSP00000380712.3:p.Ala118_Arg125del
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsp: ENSP00000405606.2:p.Ala118_Arg125del
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsp: ENSP00000344226.4:p.Ala118_Arg125del
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsp: ENSP00000380713.3:p.Ala118_Arg125del
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsp: ENSP00000403068.1:p.Ala118_Arg125del
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26200
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10069
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12321
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35028
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1871
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2811
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala118_Arg125del
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: GGCTGCGCTGGGCTGTGAGCCCCGC
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum

11-562306-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562306
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562306
    reference: chr 11
allele count: 2
allele frequency: 1.850515368530136e-5
allele num: 108078
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.352G>C
  hgvsp: ENSP00000405606.2:p.Ala118Pro
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.347G>C
  hgvsp: ENSP00000413484.2:p.Gly116Ala
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.352G>C
  hgvsp: ENSP00000380713.3:p.Ala118Pro
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.352G>C
  hgvsp: ENSP00000380712.3:p.Ala118Pro
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.275G>C
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.352G>C
  hgvsp: ENSP00000403068.1:p.Ala118Pro
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.352G>C
  hgvsp: ENSP00000344226.4:p.Ala118Pro
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5479
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10075
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12327
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26237
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2790
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12973
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala118Pro
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-562308-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562308
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562308
    reference: chr 11
allele count: 1
allele frequency: 9.256516587677726e-6
allele num: 108032
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.354T>C
  hgvsp: ENST00000397583.3:c.354T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.354T>C
  hgvsp: ENST00000344375.4:c.354T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.349T>C
  hgvsp: ENSP00000413484.2:p.Cys117Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.354T>C
  hgvsp: ENST00000454668.2:c.354T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.354T>C
  hgvsp: ENST00000397582.3:c.354T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.277T>C
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.354T>C
  hgvsp: ENST00000431809.1:c.354T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5522
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12377
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10098
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1864
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13066
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Cys117Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-562310-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562310
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562310
    reference: chr 11
allele count: 36
allele frequency: 3.340261282660332e-4
allele num: 107776
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.356C>T
  hgvsp: ENSP00000380713.3:p.Ala119Val
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.279C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.356C>T
  hgvsp: ENSP00000403068.1:p.Ala119Val
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.356C>T
  hgvsp: ENSP00000380712.3:p.Ala119Val
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.351C>T
  hgvsp: ENST00000414138.2:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.356C>T
  hgvsp: ENSP00000405606.2:p.Ala119Val
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.356C>T
  hgvsp: ENSP00000344226.4:p.Ala119Val
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 26112
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10156
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12446
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1853
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13179
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2738
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala119Val
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-562311-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562311
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562311
    reference: chr 11
allele count: 4
allele frequency: 3.757562093713598e-5
allele num: 106452
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.357G>A
  hgvsp: ENST00000344375.4:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.352G>A
  hgvsp: ENSP00000413484.2:p.Ala118Thr
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.357G>A
  hgvsp: ENST00000397583.3:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.280G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.357G>A
  hgvsp: ENST00000431809.1:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.357G>A
  hgvsp: ENST00000454668.2:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.357G>A
  hgvsp: ENST00000397582.3:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24963
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11694
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6083
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33303
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2534
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2081
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14494
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala118Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff

11-562311-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562311
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562311
    reference: chr 11
allele count: 11
allele frequency: 1.03332957577124e-4
allele num: 106452
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.357G>T
  hgvsp: ENST00000431809.1:c.357G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.357G>T
  hgvsp: ENST00000344375.4:c.357G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.357G>T
  hgvsp: ENST00000397583.3:c.357G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.357G>T
  hgvsp: ENST00000397582.3:c.357G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.280G>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.352G>T
  hgvsp: ENSP00000413484.2:p.Ala118Ser
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.357G>T
  hgvsp: ENST00000454668.2:c.357G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11694
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11249
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24963
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6083
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2081
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14494
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala118Ser
num of homozygotes: 1
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-562327-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562327
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562327
    reference: chr 11
allele count: 2
allele frequency: 2.113405330008242e-5
allele num: 94634
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.373C>T
  hgvsp: ENSP00000403068.1:p.Arg125Cys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.373C>T
  hgvsp: ENSP00000405606.2:p.Arg125Cys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.373C>T
  hgvsp: ENSP00000344226.4:p.Arg125Cys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.296C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.373C>T
  hgvsp: ENSP00000380713.3:p.Arg125Cys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.373C>T
  hgvsp: ENSP00000380712.3:p.Arg125Cys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*5C>T
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1802
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10670
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16008
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2367
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3123
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3425
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg125Cys
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

11-562328-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562328
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562328
    reference: chr 11
allele count: 60
allele frequency: 6.543646119617851e-4
allele num: 91692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.374G>A
  hgvsp: ENSP00000405606.2:p.Arg125His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*6G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.374G>A
  hgvsp: ENSP00000403068.1:p.Arg125His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.374G>A
  hgvsp: ENSP00000380713.3:p.Arg125His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.374G>A
  hgvsp: ENSP00000380712.3:p.Arg125His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.297G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.374G>A
  hgvsp: ENSP00000344226.4:p.Arg125His
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11577
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6493
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14481
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17578
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6621
  bin: 1.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 3541
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24720
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2802
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg125His
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

11-562330-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562330
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562330
    reference: chr 11
allele count: 1
allele frequency: 1.091274171722904e-5
allele num: 91636
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.376A>G
  hgvsp: ENSP00000380712.3:p.Lys126Glu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.376A>G
  hgvsp: ENSP00000344226.4:p.Lys126Glu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.299A>G
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.376A>G
  hgvsp: ENSP00000403068.1:p.Lys126Glu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.376A>G
  hgvsp: ENSP00000380713.3:p.Lys126Glu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*8A>G
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.376A>G
  hgvsp: ENSP00000405606.2:p.Lys126Glu
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6339
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25744
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1592
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18135
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2957
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3644
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1705
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys126Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
reference allele: A
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-562335-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562335
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562335
    reference: chr 11
allele count: 1
allele frequency: 1.227747084100675e-5
allele num: 81450
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.381A>G
  hgvsp: ENST00000397583.3:c.381A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.381A>G
  hgvsp: ENST00000431809.1:c.381A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.304A>G
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*13A>G
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.381A>G
  hgvsp: ENST00000397582.3:c.381A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.381A>G
  hgvsp: ENST00000344375.4:c.381A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.381A>G
  hgvsp: ENST00000454668.2:c.381A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18675
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3016
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1039
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3780
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1555
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2122
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26826
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3585
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr127Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-562339-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562339
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562339
    reference: chr 11
allele count: 53
allele frequency: 8.593293987936961e-4
allele num: 61676
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.385A>C
  hgvsp: ENSP00000380713.3:p.Thr129Pro
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.385A>C
  hgvsp: ENSP00000403068.1:p.Thr129Pro
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.385A>C
  hgvsp: ENSP00000405606.2:p.Thr129Pro
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.385A>C
  hgvsp: ENSP00000380712.3:p.Thr129Pro
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.385A>C
  hgvsp: ENSP00000344226.4:p.Thr129Pro
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*17A>C
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.308A>C
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18661
  bin: 1.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17507
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 1.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8749
  bin: 2.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7546
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4346
  bin: 1.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2734
  bin: 2.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 4549
  bin: 2.5e0
  variant carriers: 7
hgvs: p.Thr129Pro
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

11-562340-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562340
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562340
    reference: chr 11
allele count: 1
allele frequency: 1.368325989983854e-5
allele num: 73082
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.386C>T
  hgvsp: ENSP00000380713.3:p.Thr129Ile
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.309C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*18C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.386C>T
  hgvsp: ENSP00000380712.3:p.Thr129Ile
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.386C>T
  hgvsp: ENSP00000405606.2:p.Thr129Ile
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.386C>T
  hgvsp: ENSP00000403068.1:p.Thr129Ile
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.386C>T
  hgvsp: ENSP00000344226.4:p.Thr129Ile
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19029
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3684
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18364
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5338
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2661
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3212
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr129Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

11-562343-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562343
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562343
    reference: chr 11
allele count: 1
allele frequency: 1.486988847583643e-5
allele num: 67250
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.389C>T
  hgvsp: ENSP00000380713.3:p.Pro130Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.312C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.389C>T
  hgvsp: ENSP00000405606.2:p.Pro130Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.389C>T
  hgvsp: ENSP00000403068.1:p.Pro130Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.389C>T
  hgvsp: ENSP00000344226.4:p.Pro130Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*21C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.389C>T
  hgvsp: ENSP00000380712.3:p.Pro130Leu
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7659
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4060
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17856
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4279
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8654
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2109
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1072
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1399
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5907
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3080
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29712
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro130Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/11-562344-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562344
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562344
    reference: chr 11
allele count: 2
allele frequency: 3.055954527396632e-5
allele num: 65446
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.390C>A
  hgvsp: ENST00000397583.3:c.390C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.313C>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.390C>A
  hgvsp: ENST00000344375.4:c.390C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.390C>A
  hgvsp: ENST00000431809.1:c.390C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.390C>A
  hgvsp: ENST00000454668.2:c.390C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.390C>A
  hgvsp: ENST00000397582.3:c.390C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*22C>A
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17736
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4096
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1523
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29462
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1247
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1259
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8683
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2272
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2905
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro130Pro
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

11-562345-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562345
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562345
    reference: chr 11
allele count: 13
allele frequency: 1.967848384850595e-4
allele num: 66062
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.314G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.391G>A
  hgvsp: ENSP00000405606.2:p.Glu131Lys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.391G>A
  hgvsp: ENSP00000344226.4:p.Glu131Lys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*23G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.391G>A
  hgvsp: ENSP00000403068.1:p.Glu131Lys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.391G>A
  hgvsp: ENSP00000380713.3:p.Glu131Lys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.391G>A
  hgvsp: ENSP00000380712.3:p.Glu131Lys
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7769
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3721
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4403
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17535
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2861
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9409
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 30789
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2289
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu131Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-562351-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562351
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562351
    reference: chr 11
allele count: 1
allele frequency: 1.674593073883047e-5
allele num: 59716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.397G>A
  hgvsp: ENSP00000403068.1:p.Ala133Thr
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.397G>A
  hgvsp: ENSP00000405606.2:p.Ala133Thr
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.397G>A
  hgvsp: ENSP00000344226.4:p.Ala133Thr
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.397G>A
  hgvsp: ENSP00000380713.3:p.Ala133Thr
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.320G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.397G>A
  hgvsp: ENSP00000380712.3:p.Ala133Thr
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*29G>A
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16835
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22898
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2012
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2541
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1039
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30461
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala133Thr
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

11-562352-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562352
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562352
    reference: chr 11
allele count: 1
allele frequency: 1.588663298700473e-5
allele num: 62946
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.398C>T
  hgvsp: ENSP00000380712.3:p.Ala133Val
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.398C>T
  hgvsp: ENSP00000403068.1:p.Ala133Val
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.398C>T
  hgvsp: ENSP00000344226.4:p.Ala133Val
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.398C>T
  hgvsp: ENSP00000380713.3:p.Ala133Val
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*30C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.398C>T
  hgvsp: ENSP00000405606.2:p.Ala133Val
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.321C>T
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22732
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17302
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5081
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2904
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5814
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 903
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33550
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala133Val
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: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-562360-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562360
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562360
    reference: chr 11
allele count: 28
allele frequency: 4.974240540060402e-4
allele num: 56290
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.406C>T
  hgvsp: ENSP00000403068.1:p.Leu136Phe
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.406C>T
  hgvsp: ENSP00000344226.4:p.Leu136Phe
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.406C>T
  hgvsp: ENSP00000380713.3:p.Leu136Phe
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.406C>T
  hgvsp: ENSP00000380712.3:p.Leu136Phe
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*38C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.329C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.406C>T
  hgvsp: ENSP00000405606.2:p.Leu136Phe
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16473
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 24085
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2358
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 7039
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5971
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3090
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1872
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7647
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33685
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2487
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu136Phe
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-562366-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562366
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562366
    reference: chr 11
allele count: 49
allele frequency: 9.331911327797669e-4
allele num: 52508
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.412C>T
  hgvsp: ENSP00000380713.3:p.Arg138Cys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*44C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.412C>T
  hgvsp: ENSP00000344226.4:p.Arg138Cys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.412C>T
  hgvsp: ENSP00000405606.2:p.Arg138Cys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.412C>T
  hgvsp: ENSP00000403068.1:p.Arg138Cys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.412C>T
  hgvsp: ENSP00000380712.3:p.Arg138Cys
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.335C>T
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24529
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 1.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8480
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15555
  bin: 1.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 938
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9123
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg138Cys
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

11-562369-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562369
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562369
    reference: chr 11
allele count: 1
allele frequency: 2.036245163917736e-5
allele num: 49110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.415C>T
  hgvsp: ENSP00000344226.4:p.Pro139Ser
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.415C>T
  hgvsp: ENSP00000403068.1:p.Pro139Ser
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.338C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.415C>T
  hgvsp: ENSP00000380712.3:p.Pro139Ser
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.415C>T
  hgvsp: ENSP00000380713.3:p.Pro139Ser
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.415C>T
  hgvsp: ENSP00000405606.2:p.Pro139Ser
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*47C>T
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14774
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 629
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 921
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10680
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2255
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro139Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ

11-562370-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562370
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562370
    reference: chr 11
allele count: 1
allele frequency: 2.041566289657425e-5
allele num: 48982
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.416C>G
  hgvsp: ENSP00000380713.3:p.Pro139Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.416C>G
  hgvsp: ENSP00000344226.4:p.Pro139Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.339C>G
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.416C>G
  hgvsp: ENSP00000380712.3:p.Pro139Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.416C>G
  hgvsp: ENSP00000405606.2:p.Pro139Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*48C>G
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.416C>G
  hgvsp: ENSP00000403068.1:p.Pro139Arg
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14734
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24445
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1581
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10713
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2222
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2016
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6331
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro139Arg
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

11-562375-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562375
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562375
    reference: chr 11
allele count: 2
allele frequency: 4.795473073418693e-5
allele num: 41706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.344C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.421C>T
  hgvsp: ENSP00000344226.4:p.Pro141Ser
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.421C>T
  hgvsp: ENSP00000380713.3:p.Pro141Ser
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*53C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.421C>T
  hgvsp: ENSP00000380712.3:p.Pro141Ser
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.421C>T
  hgvsp: ENSP00000403068.1:p.Pro141Ser
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.421C>T
  hgvsp: ENSP00000405606.2:p.Pro141Ser
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24467
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 27701
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3602
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1941
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13562
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1632
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro141Ser
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

11-562379-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562379
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562379
    reference: chr 11
allele count: 4
allele frequency: 1.005985614405714e-4
allele num: 39762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*57C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.425C>T
  hgvsp: ENSP00000403068.1:p.Ala142Val
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.425C>T
  hgvsp: ENSP00000380712.3:p.Ala142Val
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.425C>T
  hgvsp: ENSP00000405606.2:p.Ala142Val
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.425C>T
  hgvsp: ENSP00000344226.4:p.Ala142Val
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.348C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.425C>T
  hgvsp: ENSP00000380713.3:p.Ala142Val
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4589
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11542
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24812
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13831
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5834
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14259
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1291
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 889
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1619
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala142Val
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum

11-562380-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562380
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562380
    reference: chr 11
allele count: 33
allele frequency: 8.417079018517574e-4
allele num: 39206
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.426G>A
  hgvsp: ENST00000397583.3:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.426G>A
  hgvsp: ENST00000431809.1:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.426G>A
  hgvsp: ENST00000397582.3:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.426G>A
  hgvsp: ENST00000344375.4:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.426G>A
  hgvsp: ENST00000454668.2:c.426G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*58G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.349G>A
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 24972
  bin: 7.5e0
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14277
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11139
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14665
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1745
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 896
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2591
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala142Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-562383-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562383
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562383
    reference: chr 11
allele count: 1
allele frequency: 2.717095967829584e-5
allele num: 36804
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.429C>A
  hgvsp: ENST00000397583.3:c.429C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.429C>A
  hgvsp: ENST00000344375.4:c.429C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.429C>A
  hgvsp: ENST00000397582.3:c.429C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.352C>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.429C>A
  hgvsp: ENST00000431809.1:c.429C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*61C>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.429C>A
  hgvsp: ENST00000454668.2:c.429C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15854
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1688
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3111
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16304
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala143Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/11-562398-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562398
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562398
    reference: chr 11
allele count: 1
allele frequency: 3.155569580309246e-5
allele num: 31690
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.444A>C
  hgvsp: ENST00000344375.4:c.444A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*76A>C
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.444A>C
  hgvsp: ENST00000431809.1:c.444A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.444A>C
  hgvsp: ENST00000454668.2:c.444A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.14A>C
  hgvsp: ENST00000531112.1:c.14A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.444A>C
  hgvsp: ENST00000397582.3:c.444A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.444A>C
  hgvsp: ENST00000397583.3:c.444A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.367A>C
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7795
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21011
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21744
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2310
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr148Thr
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

11-562399-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562399
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562399
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 31508
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.445C>T
  hgvsp: ENSP00000380712.3:p.Pro149Ser
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.445C>T
  hgvsp: ENSP00000344226.4:p.Pro149Ser
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.445C>T
  hgvsp: ENSP00000403068.1:p.Pro149Ser
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.445C>T
  hgvsp: ENSP00000380713.3:p.Pro149Ser
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.15C>T
  hgvsp: ENSP00000435885.1:p.Pro6Ser
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*77C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.445C>T
  hgvsp: ENSP00000405606.2:p.Pro149Ser
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.368C>T
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21484
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21017
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22296
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro149Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

11-562403-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562403
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562403
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 30046
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.449G>A
  hgvsp: ENSP00000380713.3:p.Gly150Asp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.449G>A
  hgvsp: ENSP00000403068.1:p.Gly150Asp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*81G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.372G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.449G>A
  hgvsp: ENSP00000380712.3:p.Gly150Asp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.449G>A
  hgvsp: ENSP00000344226.4:p.Gly150Asp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.449G>A
  hgvsp: ENSP00000405606.2:p.Gly150Asp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.19G>A
  hgvsp: ENSP00000435885.1:p.Gly7Asp
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20013
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22982
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6789
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23964
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19607
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2026
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5923
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1020
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly150Asp
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

11-562408-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562408
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562408
    reference: chr 11
allele count: 81
allele frequency: 3.110838005991243e-3
allele num: 26038
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.377T>C
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.24T>C
  hgvsp: ENSP00000435885.1:p.Cys9Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.454T>C
  hgvsp: ENSP00000380712.3:p.Cys152Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.454T>C
  hgvsp: ENSP00000405606.2:p.Cys152Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.454T>C
  hgvsp: ENSP00000380713.3:p.Cys152Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.454T>C
  hgvsp: ENSP00000403068.1:p.Cys152Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.454T>C
  hgvsp: ENSP00000344226.4:p.Cys152Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*86T>C
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 1.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17093
  bin: 7.5e0
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 26320
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3156
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 9.75e1
  variant carriers: 85
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 2.75e1
  variant carriers: 4
hgvs: p.Cys152Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-562416-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562416
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562416
    reference: chr 11
allele count: 1
allele frequency: 4.351988858908521e-5
allele num: 22978
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.32C>A
  hgvsp: ENSP00000435885.1:p.Asp11Glu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.462C>A
  hgvsp: ENSP00000344226.4:p.Asp154Glu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.462C>A
  hgvsp: ENSP00000380713.3:p.Asp154Glu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*94C>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.462C>A
  hgvsp: ENSP00000405606.2:p.Asp154Glu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.462C>A
  hgvsp: ENSP00000380712.3:p.Asp154Glu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.385C>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.462C>A
  hgvsp: ENSP00000403068.1:p.Asp154Glu
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15109
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2016
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3430
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp154Glu
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

11-562416-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562416
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562416
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 22978
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.462C>T
  hgvsp: ENST00000431809.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*94C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.462C>T
  hgvsp: ENST00000454668.2:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.462C>T
  hgvsp: ENST00000397583.3:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.462C>T
  hgvsp: ENST00000397582.3:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.32C>T
  hgvsp: ENST00000531112.1:c.32C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.462C>T
  hgvsp: ENST00000344375.4:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.385C>T
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: synonymous
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15109
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28561
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3430
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp154Asp
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

11-562419-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562419
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562419
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 22798
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.465G>T
  hgvsp: ENST00000344375.4:c.465G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*97G>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.388G>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.465G>T
  hgvsp: ENST00000397583.3:c.465G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.35G>T
  hgvsp: ENST00000531112.1:c.35G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.465G>T
  hgvsp: ENST00000397582.3:c.465G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.465G>T
  hgvsp: ENST00000454668.2:c.465G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.465G>T
  hgvsp: ENST00000431809.1:c.465G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28452
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14886
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9285
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28960
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu155Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

11-562420-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562420
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562420
    reference: chr 11
allele count: 1
allele frequency: 4.38288920056101e-5
allele num: 22816
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.466C>T
  hgvsp: ENSP00000344226.4:p.Arg156Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*98C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.389C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.466C>T
  hgvsp: ENSP00000380713.3:p.Arg156Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.36C>T
  hgvsp: ENSP00000435885.1:p.Arg13Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.466C>T
  hgvsp: ENSP00000403068.1:p.Arg156Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.466C>T
  hgvsp: ENSP00000405606.2:p.Arg156Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.466C>T
  hgvsp: ENSP00000380712.3:p.Arg156Trp
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28521
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14856
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2589
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg156Trp
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

11-562420-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562420
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562419
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 22816
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.470delG
  hgvsp: ENSP00000405606.2:p.Gly157AlafsTer40
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.470delG
  hgvsp: ENSP00000403068.1:p.Gly157AlafsTer40
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.470delG
  hgvsp: ENSP00000380712.3:p.Gly157AlafsTer40
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.470delG
  hgvsp: ENSP00000380713.3:p.Gly157AlafsTer40
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.470delG
  hgvsp: ENSP00000344226.4:p.Gly157AlafsTer40
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*102delG
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.393delG
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.40delG
  hgvsp: ENSP00000435885.1:p.Gly14AlafsTer40
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 4500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28521
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14856
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5891
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9443
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly157AlafsTer40
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: CG
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

11-562421-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562421
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562421
    reference: chr 11
allele count: 1945
allele frequency: 8.644444444444445e-2
allele num: 22500
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.467G>A
  hgvsp: ENSP00000405606.2:p.Arg156Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.467G>A
  hgvsp: ENSP00000344226.4:p.Arg156Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.37G>A
  hgvsp: ENSP00000435885.1:p.Arg13Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*99G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.390G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.467G>A
  hgvsp: ENSP00000380713.3:p.Arg156Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.467G>A
  hgvsp: ENSP00000403068.1:p.Arg156Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.467G>A
  hgvsp: ENSP00000380712.3:p.Arg156Gln
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 2.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.75e1
  variant carriers: 186
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 1.25e1
  variant carriers: 549
genotype depth: GenotypeDepth
  all individuals: 28094
  bin: 2.5e0
  variant carriers: 571
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.25e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 14452
  bin: 7.5e0
  variant carriers: 2050
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 4001
  bin: 2.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.25e1
  variant carriers: 41
genotype quality: GenotypeQuality
  all individuals: 890
  bin: 6.75e1
  variant carriers: 107
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 7.25e1
  variant carriers: 55
genotype quality: GenotypeQuality
  all individuals: 2009
  bin: 1.75e1
  variant carriers: 251
genotype quality: GenotypeQuality
  all individuals: 26918
  bin: 7.5e0
  variant carriers: 211
genotype quality: GenotypeQuality
  all individuals: 3504
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 9.75e1
  variant carriers: 2203
hgvs: p.Arg156Gln
num of homozygotes: 116
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

11-562421-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562421
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562421
    reference: chr 11
allele count: 3
allele frequency: 1.333333333333333e-4
allele num: 22500
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.37G>C
  hgvsp: ENSP00000435885.1:p.Arg13Pro
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.467G>C
  hgvsp: ENSP00000344226.4:p.Arg156Pro
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.467G>C
  hgvsp: ENSP00000403068.1:p.Arg156Pro
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.467G>C
  hgvsp: ENSP00000380713.3:p.Arg156Pro
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.390G>C
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*99G>C
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.467G>C
  hgvsp: ENSP00000380712.3:p.Arg156Pro
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.467G>C
  hgvsp: ENSP00000405606.2:p.Arg156Pro
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14452
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28094
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5455
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2009
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg156Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

11-562424-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562424
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562424
    reference: chr 11
allele count: 10
allele frequency: 4.612971676353907e-4
allele num: 21678
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.470G>C
  hgvsp: ENSP00000380712.3:p.Gly157Ala
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*102G>C
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.470G>C
  hgvsp: ENSP00000380713.3:p.Gly157Ala
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.40G>C
  hgvsp: ENSP00000435885.1:p.Gly14Ala
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.470G>C
  hgvsp: ENSP00000344226.4:p.Gly157Ala
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.470G>C
  hgvsp: ENSP00000405606.2:p.Gly157Ala
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.470G>C
  hgvsp: ENSP00000403068.1:p.Gly157Ala
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.393G>C
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12394
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4212
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30808
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1855
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1748
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly157Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

11-562427-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562427
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562427
    reference: chr 11
allele count: 1
allele frequency: 4.755564009891573e-5
allele num: 21028
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*105T>G
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.473T>G
  hgvsp: ENSP00000380713.3:p.Leu158Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.473T>G
  hgvsp: ENSP00000405606.2:p.Leu158Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.43T>G
  hgvsp: ENSP00000435885.1:p.Leu15Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.473T>G
  hgvsp: ENSP00000380712.3:p.Leu158Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.473T>G
  hgvsp: ENSP00000344226.4:p.Leu158Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.473T>G
  hgvsp: ENSP00000403068.1:p.Leu158Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.396T>G
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30826
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11735
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 30570
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6158
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1931
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu158Arg
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

11-562437-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562437
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562437
    reference: chr 11
allele count: 3601
allele frequency: 1.73843777155547e-1
allele num: 20714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.483G>A
  hgvsp: ENST00000431809.1:c.483G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.53G>A
  hgvsp: ENST00000531112.1:c.53G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.483G>A
  hgvsp: ENST00000454668.2:c.483G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.483G>A
  hgvsp: ENST00000344375.4:c.483G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.483G>A
  hgvsp: ENST00000397582.3:c.483G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.483G>A
  hgvsp: ENST00000397583.3:c.483G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*115G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.406G>A
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 2.25e1
  variant carriers: 200
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.75e1
  variant carriers: 275
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.75e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 9.75e1
  variant carriers: 659
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 3.25e1
  variant carriers: 126
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 9.25e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 5.75e1
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.75e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.25e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 2.75e1
  variant carriers: 171
genotype depth: GenotypeDepth
  all individuals: 27776
  bin: 2.5e0
  variant carriers: 1837
genotype depth: GenotypeDepth
  all individuals: 10301
  bin: 7.5e0
  variant carriers: 4127
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.25e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 1.25e1
  variant carriers: 718
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.25e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 106
genotype quality: GenotypeQuality
  all individuals: 990
  bin: 6.75e1
  variant carriers: 313
genotype quality: GenotypeQuality
  all individuals: 5576
  bin: 6.25e1
  variant carriers: 344
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 1.75e1
  variant carriers: 653
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 9.25e1
  variant carriers: 330
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 3.25e1
  variant carriers: 306
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 5.75e1
  variant carriers: 284
hgvs: p.Arg161Arg
num of homozygotes: 325
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

11-562451-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562451
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562451
    reference: chr 11
allele count: 42
allele frequency: 2.178197282439581e-3
allele num: 19282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*129C>G
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.497C>G
  hgvsp: ENSP00000403068.1:p.Ala166Gly
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.497C>G
  hgvsp: ENSP00000344226.4:p.Ala166Gly
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.67C>G
  hgvsp: ENSP00000435885.1:p.Ala23Gly
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.497C>G
  hgvsp: ENSP00000380712.3:p.Ala166Gly
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.497C>G
  hgvsp: ENSP00000380713.3:p.Ala166Gly
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.420C>G
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.497C>G
  hgvsp: ENSP00000405606.2:p.Ala166Gly
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32436
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 2.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2954
  bin: 2.25e1
  variant carriers: 1
hgvs: p.Ala166Gly
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ

11-562455-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562455
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562455
    reference: chr 11
allele count: 1
allele frequency: 5.206706237634073e-5
allele num: 19206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.71G>A
  hgvsp: ENST00000531112.1:c.71G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*133G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.501G>A
  hgvsp: ENST00000397583.3:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.501G>A
  hgvsp: ENST00000431809.1:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.501G>A
  hgvsp: ENST00000397582.3:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000099849
  ensembl transcript: ENST00000524468
  gene symbol: RASSF7
  hgvsc: ENST00000524468.1:n.424G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.501G>A
  hgvsp: ENST00000344375.4:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.501G>A
  hgvsp: ENST00000454668.2:c.501G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3509
  bin: 2.75e1
  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: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2751
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7059
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu167Glu
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

11-562460-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562460
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562460
    reference: chr 11
allele count: 1
allele frequency: 5.226845076311938e-5
allele num: 19132
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*138T>G
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.506T>G
  hgvsp: ENSP00000403068.1:p.Leu169Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.506T>G
  hgvsp: ENSP00000380713.3:p.Leu169Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.76T>G
  hgvsp: ENSP00000435885.1:p.Leu26Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.506T>G
  hgvsp: ENSP00000380712.3:p.Leu169Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.506T>G
  hgvsp: ENSP00000344226.4:p.Leu169Arg
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.506T>G
  hgvsp: ENSP00000405606.2:p.Leu169Arg
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3411
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1095
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu169Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ

11-562461-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562461
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562461
    reference: chr 11
allele count: 1
allele frequency: 5.249343832020998e-5
allele num: 19050
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.507G>A
  hgvsp: ENST00000431809.1:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.507G>A
  hgvsp: ENST00000397583.3:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.77G>A
  hgvsp: ENST00000531112.1:c.77G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.507G>A
  hgvsp: ENST00000454668.2:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.507G>A
  hgvsp: ENST00000397582.3:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*139G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.507G>A
  hgvsp: ENST00000344375.4:c.507G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31016
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1090
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2414
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu169Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-562469-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562469
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562469
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 18930
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.85A>C
  hgvsp: ENSP00000435885.1:p.Glu29Ala
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.515A>C
  hgvsp: ENSP00000380713.3:p.Glu172Ala
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.515A>C
  hgvsp: ENSP00000380712.3:p.Glu172Ala
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.515A>C
  hgvsp: ENSP00000403068.1:p.Glu172Ala
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.515A>C
  hgvsp: ENSP00000344226.4:p.Glu172Ala
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*147A>C
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.515A>C
  hgvsp: ENSP00000405606.2:p.Glu172Ala
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30064
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6968
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2243
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu172Ala
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ

11-562473-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562473
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562473
    reference: chr 11
allele count: 11
allele frequency: 5.828740991945739e-4
allele num: 18872
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*151C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.519C>T
  hgvsp: ENST00000431809.1:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.89C>T
  hgvsp: ENST00000531112.1:c.89C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.519C>T
  hgvsp: ENST00000344375.4:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.519C>T
  hgvsp: ENST00000454668.2:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.519C>T
  hgvsp: ENST00000397583.3:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.519C>T
  hgvsp: ENST00000397582.3:c.519C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 29235
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 2.25e1
  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 quality: GenotypeQuality
  all individuals: 26493
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2125
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2980
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala173Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

11-562480-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562480
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562480
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 18750
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.526G>C
  hgvsp: ENSP00000344226.4:p.Glu176Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.526G>C
  hgvsp: ENSP00000380713.3:p.Glu176Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.526G>C
  hgvsp: ENSP00000380712.3:p.Glu176Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.526G>C
  hgvsp: ENSP00000403068.1:p.Glu176Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.96G>C
  hgvsp: ENSP00000435885.1:p.Glu33Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*158G>C
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.526G>C
  hgvsp: ENSP00000405606.2:p.Glu176Gln
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 28287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3852
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25633
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Glu176Gln
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

11-562482-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562482
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562482
    reference: chr 11
allele count: 1
allele frequency: 5.356760231412042e-5
allele num: 18668
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.528G>A
  hgvsp: ENST00000431809.1:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.528G>A
  hgvsp: ENST00000397583.3:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.528G>A
  hgvsp: ENST00000454668.2:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.98G>A
  hgvsp: ENST00000531112.1:c.98G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*160G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.528G>A
  hgvsp: ENST00000344375.4:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.528G>A
  hgvsp: ENST00000397582.3:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27040
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 7.5e0
  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: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1859
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23686
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu176Glu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

11-562495-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562495
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562495
    reference: chr 11
allele count: 2
allele frequency: 1.088613106901807e-4
allele num: 18372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.541C>T
  hgvsp: ENSP00000403068.1:p.Arg181Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.541C>T
  hgvsp: ENSP00000405606.2:p.Arg181Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.541C>T
  hgvsp: ENSP00000380712.3:p.Arg181Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.541C>T
  hgvsp: ENSP00000380713.3:p.Arg181Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*173C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.111C>T
  hgvsp: ENSP00000435885.1:p.Arg38Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.541C>T
  hgvsp: ENSP00000344226.4:p.Arg181Trp
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6456
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21842
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg181Trp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

11-562503-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562503
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562503
    reference: chr 11
allele count: 1
allele frequency: 5.50478916657492e-5
allele num: 18166
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.549G>C
  hgvsp: ENSP00000403068.1:p.Gln183His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.549G>C
  hgvsp: ENSP00000405606.2:p.Gln183His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*181G>C
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.119G>C
  hgvsp: ENSP00000435885.1:p.Gln40His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.549G>C
  hgvsp: ENSP00000380713.3:p.Gln183His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.549G>C
  hgvsp: ENSP00000380712.3:p.Gln183His
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.549G>C
  hgvsp: ENSP00000344226.4:p.Gln183His
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23880
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3224
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6359
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1862
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln183His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-562507-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562507
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562507
    reference: chr 11
allele count: 1
allele frequency: 5.536485439043296e-5
allele num: 18062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.553C>T
  hgvsp: ENSP00000344226.4:p.Arg185Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.553C>T
  hgvsp: ENSP00000405606.2:p.Arg185Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.553C>T
  hgvsp: ENSP00000403068.1:p.Arg185Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.553C>T
  hgvsp: ENSP00000380713.3:p.Arg185Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.123C>T
  hgvsp: ENSP00000435885.1:p.Arg42Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.553C>T
  hgvsp: ENSP00000380712.3:p.Arg185Trp
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*185C>T
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23122
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3446
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3666
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1862
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg185Trp
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

11-562508-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562508
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562508
    reference: chr 11
allele count: 3
allele frequency: 1.67935512763099e-4
allele num: 17864
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.554G>A
  hgvsp: ENSP00000405606.2:p.Arg185Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.124G>A
  hgvsp: ENSP00000435885.1:p.Arg42Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.554G>A
  hgvsp: ENSP00000380713.3:p.Arg185Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*186G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.554G>A
  hgvsp: ENSP00000403068.1:p.Arg185Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.554G>A
  hgvsp: ENSP00000380712.3:p.Arg185Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.554G>A
  hgvsp: ENSP00000344226.4:p.Arg185Gln
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22383
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6095
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18288
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg185Gln
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

11-562513-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562513
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562513
    reference: chr 11
allele count: 1
allele frequency: 5.613562366677894e-5
allele num: 17814
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.559C>T
  hgvsp: ENSP00000380712.3:p.Arg187Ter
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.559C>T
  hgvsp: ENSP00000380713.3:p.Arg187Ter
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*191C>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.559C>T
  hgvsp: ENSP00000344226.4:p.Arg187Ter
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.559C>T
  hgvsp: ENSP00000403068.1:p.Arg187Ter
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.129C>T
  hgvsp: ENSP00000435885.1:p.Arg44Ter
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.559C>T
  hgvsp: ENSP00000405606.2:p.Arg187Ter
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22845
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19565
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3366
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1919
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg187Ter
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

11-562514-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562514
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562514
    reference: chr 11
allele count: 2
allele frequency: 1.125365743866757e-4
allele num: 17772
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.560G>A
  hgvsp: ENSP00000380712.3:p.Arg187Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.560G>A
  hgvsp: ENSP00000405606.2:p.Arg187Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.560G>A
  hgvsp: ENSP00000344226.4:p.Arg187Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.560G>A
  hgvsp: ENSP00000403068.1:p.Arg187Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*192G>A
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.130G>A
  hgvsp: ENSP00000435885.1:p.Arg44Gln
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.560G>A
  hgvsp: ENSP00000380713.3:p.Arg187Gln
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22672
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 2.25e1
  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: 933
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6128
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg187Gln
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

11-562514-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562514
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562514
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 17772
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.560G>T
  hgvsp: ENSP00000405606.2:p.Arg187Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.560G>T
  hgvsp: ENSP00000344226.4:p.Arg187Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*192G>T
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.560G>T
  hgvsp: ENSP00000403068.1:p.Arg187Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.560G>T
  hgvsp: ENSP00000380713.3:p.Arg187Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.130G>T
  hgvsp: ENSP00000435885.1:p.Arg44Leu
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.560G>T
  hgvsp: ENSP00000380712.3:p.Arg187Leu
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: missense
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22672
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 7.5e0
  variant carriers: 1
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: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 956
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6128
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1938
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg187Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

11-562518-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 562518
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 562518
    reference: chr 11
allele count: 1
allele frequency: 5.647803004631199e-5
allele num: 17706
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000435885
  ensembl transcript: ENST00000531112
  gene symbol: RASSF7
  hgvsc: ENST00000531112.1:c.134G>A
  hgvsp: ENST00000531112.1:c.134G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380713
  ensembl transcript: ENST00000397583
  gene symbol: RASSF7
  hgvsc: ENST00000397583.3:c.564G>A
  hgvsp: ENST00000397583.3:c.564G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000380712
  ensembl transcript: ENST00000397582
  gene symbol: RASSF7
  hgvsc: ENST00000397582.3:c.564G>A
  hgvsp: ENST00000397582.3:c.564G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000344226
  ensembl transcript: ENST00000344375
  gene symbol: RASSF7
  hgvsc: ENST00000344375.4:c.564G>A
  hgvsp: ENST00000344375.4:c.564G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000405606
  ensembl transcript: ENST00000454668
  gene symbol: RASSF7
  hgvsc: ENST00000454668.2:c.564G>A
  hgvsp: ENST00000454668.2:c.564G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000403068
  ensembl transcript: ENST00000431809
  gene symbol: RASSF7
  hgvsc: ENST00000431809.1:c.564G>A
  hgvsp: ENST00000431809.1:c.564G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1166
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000099849
  ensembl protein: ENSP00000413484
  ensembl transcript: ENST00000414138
  gene symbol: RASSF7
  hgvsc: ENST00000414138.2:c.*196G>A
  variant of: http://identifiers.org/hgnc/1166
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22662
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu188Glu
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 206
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5151
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540309910353963e-5
allele num: 64922
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10084
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16254
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.08e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.7e-1

MQ
type: SiteQuality
SIO_000300: 5.93e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 1.434484e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.812e0

GenotypeQuality
all individuals: 31
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 865
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 50318
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.529051987767584e-4
allele num: 6540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.741258741258741e-5
allele num: 11440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.080524921446614e-5
allele num: 64924
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10082
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16272
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.48e0

VQSLOD
type: SiteQuality
SIO_000300: -1.819e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.4e-2

QD
type: SiteQuality
SIO_000300: 2.261e1

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

FS
type: SiteQuality
SIO_000300: 1.6897e1

DP
type: SiteQuality
SIO_000300: 1.434888e6

MQ
type: SiteQuality
SIO_000300: 5.948e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.71e-1

GenotypeQuality
all individuals: 50121
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5136
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 994
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64860
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.147792942333702e-5
allele num: 16266
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10072
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e-1

FS
type: SiteQuality
SIO_000300: 7.542e0

VQSLOD
type: SiteQuality
SIO_000300: -6.33e-1

QD
type: SiteQuality
SIO_000300: 8.84e0

MQRankSum
type: SiteQuality
SIO_000300: -1.037e0

DP
type: SiteQuality
SIO_000300: 1.43195e6

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5127
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50188
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 101
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16268
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.625204279855694e-5
allele num: 64862
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10072
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.13e-1

FS
type: SiteQuality
SIO_000300: 5.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

DP
type: SiteQuality
SIO_000300: 1.432118e6

QD
type: SiteQuality
SIO_000300: 1.325e1

GenotypeQuality
all individuals: 112
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5119
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 991
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64840
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.332633543270352e-4
allele num: 8574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10062
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.147037128104254e-5
allele num: 16268
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

FS
type: SiteQuality
SIO_000300: 1.342e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.099e0

DP
type: SiteQuality
SIO_000300: 1.431681e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.04e-1

QD
type: SiteQuality
SIO_000300: 1.405e1

MQRankSum
type: SiteQuality
SIO_000300: -3.91e-1

GenotypeQuality
all individuals: 321
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 856
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 990
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5094
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 1.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64778
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10050
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.765778401122019e-5
allele num: 11408
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16238
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.44e-1

DP
type: SiteQuality
SIO_000300: 1.42849e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.164e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

QD
type: SiteQuality
SIO_000300: 1.452e1

MQRankSum
type: SiteQuality
SIO_000300: 2.04e0

VQSLOD
type: SiteQuality
SIO_000300: -4.186e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 5039
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49044
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.005631536604988e-4
allele num: 9944
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16146
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11338
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: -1.01e-1

QD
type: SiteQuality
SIO_000300: 7.25e0

MQRankSum
type: SiteQuality
SIO_000300: -2.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.416676e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.41e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 8

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.830801836806782e-5
allele num: 11324
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9928
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64374
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.19480215406228e-4
allele num: 8542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16136
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

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

DP
type: SiteQuality
SIO_000300: 1.414971e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.02e-1

BaseQRankSum
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SIO_000300: -2.064e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.21e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.014816318246397e-4
allele num: 9854
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11262
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16048
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.560987793075458e-5
allele num: 64062
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.305e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.981e0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e-1

DP
type: SiteQuality
SIO_000300: 1.403165e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 9.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.4e-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
all individuals: 91
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6310
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9670
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11158
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63396
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

DP
type: SiteQuality
SIO_000300: 1.38036e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-2

GenotypeQuality
all individuals: 157
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8324
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15652
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.602050624799744e-5
allele num: 62420
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6216
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11050
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.493e0

MQRankSum
type: SiteQuality
SIO_000300: -1.126e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.45e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.628e-1

QD
type: SiteQuality
SIO_000300: 1.273e1

DP
type: SiteQuality
SIO_000300: 1.343886e6

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 1063
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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: 312
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 809
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GenotypeQuality
all individuals: 229
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.076426264800861e-4
allele num: 9290
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8192
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6106
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61452
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

QD
type: SiteQuality
SIO_000300: 8.91e0

FS
type: SiteQuality
SIO_000300: 3.023e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

DP
type: SiteQuality
SIO_000300: 1.306193e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.097e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.492e0

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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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10886
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9282
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.466632177961717e-5
allele num: 15464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61432
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.26e0

MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 2.9e-2

FS
type: SiteQuality
SIO_000300: 4.938e0

DP
type: SiteQuality
SIO_000300: 1.305349e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.5e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e0

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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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6098
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.627816121890871e-5
allele num: 61432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10886
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.536e0

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.305349e6

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

MQ
type: SiteQuality
SIO_000300: 5.925e1

FS
type: SiteQuality
SIO_000300: 4.938e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.5e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10836
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.634253963065861e-5
allele num: 61190
num of homozygotes: 0

African
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allele count: 0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -4.37e-1

FS
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e-1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8118
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.924006171421068e-5
allele num: 60926
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.711263685284839e-4
allele num: 10778
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: 0.0e0
allele num: 15390
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

DP
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 7.26e-1

MQ
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ReadPosRankSum
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QD
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SIO_000300: 1.362e1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 10478
num of homozygotes: 0

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

South Asian
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allele frequency: 1.326084073730274e-4
allele num: 15082
num of homozygotes: 0

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

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

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e-1

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

MQRankSum
type: SiteQuality
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DP
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele num: 15080
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Latino
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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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European (Non-Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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VQSLOD
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BaseQRankSum
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DP
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InbreedingCoeff
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QD
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MQ
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FS
type: SiteQuality
SIO_000300: 4.058e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 5858
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 7828
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.381920254320403e-5
allele num: 59138
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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South Asian
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MQRankSum
type: SiteQuality
SIO_000300: -9.61e-1

ClippingRankSum
type: SiteQuality
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FS
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SIO_000300: 3.728e0

DP
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ReadPosRankSum
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.053e-1

QD
type: SiteQuality
SIO_000300: 1.148e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

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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variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15076
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10466
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8898
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5836
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7836
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.05e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.735e0

DP
type: SiteQuality
SIO_000300: 1.208102e6

QD
type: SiteQuality
SIO_000300: 7.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-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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South Asian
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allele count: 2
allele frequency: 1.328550551348479e-4
allele num: 15054
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.128668171557562e-4
allele num: 8860
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5828
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.913875598086124e-4
allele num: 10450
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.391094984570518e-5
allele num: 58978
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 796
num of homozygotes: 0

East Asian
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allele count: 29
allele frequency: 3.713188220230474e-3
allele num: 7810
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-2

QD
type: SiteQuality
SIO_000300: 1.266e1

MQ
type: SiteQuality
SIO_000300: 5.938e1

MQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

VQSLOD
type: SiteQuality
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FS
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SIO_000300: 0.0e0

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-2

BaseQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5726
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.299714062906161e-4
allele num: 7694
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African
type: Population
allele count: 1
allele frequency: 1.140510948905109e-4
allele num: 8768
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14918
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.717327837884252e-5
allele num: 58230
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Latino
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allele count: 1
allele frequency: 9.669309611293753e-5
allele num: 10342
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QD
type: SiteQuality
SIO_000300: 1.256e1

ReadPosRankSum
type: SiteQuality
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VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.4e-2

FS
type: SiteQuality
SIO_000300: 1.288e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.433e0

DP
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SIO_000300: 1.179956e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

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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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5726
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

European (Non-Finnish)
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allele count: 7
allele frequency: 1.202129486518976e-4
allele num: 58230
num of homozygotes: 1

Latino
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allele frequency: 2.900792883388126e-4
allele num: 10342
num of homozygotes: 0

African
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East Asian
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Other
type: Population
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allele num: 774
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VQSLOD
type: SiteQuality
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FS
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DP
type: SiteQuality
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MQRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.948482132418846e-5
allele num: 51322
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Latino
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FS
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InbreedingCoeff
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DP
type: SiteQuality
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MQRankSum
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QD
type: SiteQuality
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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allele frequency: 4.071542823905773e-3
allele num: 13754
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European (Non-Finnish)
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allele count: 2
allele frequency: 4.027386226339106e-5
allele num: 49660
num of homozygotes: 0

Latino
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East Asian
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Other
type: Population
allele count: 2
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allele num: 666
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European (Finnish)
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allele count: 0
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MQ
type: SiteQuality
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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QD
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DP
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

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

GenotypeQuality
all individuals: 494
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3269
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8804
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4810
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.538935056940597e-4
allele num: 6498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7518
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.45177e5

FS
type: SiteQuality
SIO_000300: 7.656e0

QD
type: SiteQuality
SIO_000300: 4.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.899999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.56e0

MQRankSum
type: SiteQuality
SIO_000300: 3.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.888e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.2e-3

GenotypeQuality
all individuals: 516
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4573
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1210
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11161
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1106
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 818
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 277
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5784
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7852
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.591861524445795e-5
allele num: 13172
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3996
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

QD
type: SiteQuality
SIO_000300: 1.189e1

VQSLOD
type: SiteQuality
SIO_000300: 8.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.13e-2

FS
type: SiteQuality
SIO_000300: 1.264e0

DP
type: SiteQuality
SIO_000300: 8.5465e5

MQRankSum
type: SiteQuality
SIO_000300: 3.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

GenotypeQuality
all individuals: 2222
bin: 3.25e1
variant carriers: 7

GenotypeQuality
all individuals: 690
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 928
bin: 4.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1087
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 6084
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 2789
bin: 1.25e1
variant carriers: 6

GenotypeQuality
all individuals: 23285
bin: 2.25e1
variant carriers: 5

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1329
bin: 3.75e1
variant carriers: 9

GenotypeQuality
all individuals: 713
bin: 4.25e1
variant carriers: 5

African
type: Population
allele count: 1
allele frequency: 2.148689299527288e-4
allele num: 4654
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 4.270584215920738e-4
allele num: 11708
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.855287569573284e-4
allele num: 5390
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 1.093493712411154e-3
allele num: 3658
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 4.115710253998119e-4
allele num: 34016
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 28
allele frequency: 1.569506726457399e-2
allele num: 1784
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.512e0

VQSLOD
type: SiteQuality
SIO_000300: -6.876e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.17e-2

DP
type: SiteQuality
SIO_000300: 8.08584e5

FS
type: SiteQuality
SIO_000300: 3.6495e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

QD
type: SiteQuality
SIO_000300: 5.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.034e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 297
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30679
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10596
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1290
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1243
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38960
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7048
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.954183900731785e-5
allele num: 12572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3192
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5748
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5024
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.249e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.163e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

QD
type: SiteQuality
SIO_000300: 5.3e0

DP
type: SiteQuality
SIO_000300: 8.03576e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.33e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.78e-1

GenotypeQuality
all individuals: 702
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2600
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1329
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5108
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 480
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.813097783278947e-5
allele num: 35548
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.118000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.236000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.414e0

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

QD
type: SiteQuality
SIO_000300: 8.31e0

DP
type: SiteQuality
SIO_000300: 7.64546e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.41e-2

GenotypeQuality
all individuals: 1030
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5937
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2355
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 60
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 281
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 468
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4336
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.042483660130719e-4
allele num: 4896
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.271298593879239e-5
allele num: 12090
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34890
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.78e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 5.9e0

VQSLOD
type: SiteQuality
SIO_000300: 5.34e-1

QD
type: SiteQuality
SIO_000300: 1.095e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.83e-1

DP
type: SiteQuality
SIO_000300: 7.61842e5

GenotypeQuality
all individuals: 1339
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1517
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6026
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 6.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2664
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 3.300874731803928e-4
allele num: 12118
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35088
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5012
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.17359568390987e-4
allele num: 6302
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 1.592356687898089e-3
allele num: 4396
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.57416e5

FS
type: SiteQuality
SIO_000300: 5.37e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.041e0

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.9e-2

QD
type: SiteQuality
SIO_000300: 1.079e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-2

GenotypeQuality
all individuals: 6031
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2399
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8062
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 258
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5654
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.187962254526906e-5
allele num: 31368
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2276
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

DP
type: SiteQuality
SIO_000300: 7.24718e5

MQRankSum
type: SiteQuality
SIO_000300: -1.27e0

QD
type: SiteQuality
SIO_000300: 1.164e1

MQ
type: SiteQuality
SIO_000300: 5.883e1

FS
type: SiteQuality
SIO_000300: 3.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.738e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.27e0

GenotypeQuality
all individuals: 372
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2085
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2690
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1043
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8936
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2768
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.004446580939791e-5
allele num: 33284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11714
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5798
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4916
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4006
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

DP
type: SiteQuality
SIO_000300: 7.37394e5

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

QD
type: SiteQuality
SIO_000300: 1.156e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.54e-2

GenotypeQuality
all individuals: 288
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 944
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7391
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 256
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 969
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 189
bin: 9.75e1
variant carriers: 28

GenotypeQuality
all individuals: 1823
bin: 1.75e1
variant carriers: 1

Latino
type: Population
allele count: 16
allele frequency: 3.17208564631245e-3
allele num: 5044
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

African
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allele count: 1
allele frequency: 2.255299954894001e-4
allele num: 4434
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 11
allele frequency: 3.748125937031484e-4
allele num: 29348
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

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.74e-1

MQRankSum
type: SiteQuality
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MQ
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SIO_000300: 6.0e1

QD
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.88e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.954e0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3190
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 48
allele frequency: 1.769911504424779e-3
allele num: 27120
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10870
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 4212
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 4.549590536851683e-4
allele num: 2198
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
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InbreedingCoeff
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FS
type: SiteQuality
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VQSLOD
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MQRankSum
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MQ
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 6.59306e5

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

South Asian
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allele frequency: 9.441087613293051e-5
allele num: 10592
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4112
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2020
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African
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 378
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 25166
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
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QD
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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DP
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SIO_000300: 6.33073e5

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.015e1

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2016
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25124
num of homozygotes: 0

South Asian
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allele frequency: 9.455370650529501e-5
allele num: 10576
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.8447e1

QD
type: SiteQuality
SIO_000300: 1.421e1

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

DP
type: SiteQuality
SIO_000300: 6.32488e5

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.46e-2

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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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2232
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10074
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.059975520195838e-4
allele num: 3268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1476
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 330
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African
type: Population
allele count: 1
allele frequency: 2.888503755054881e-4
allele num: 3462
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 20864
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.92637e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.262e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.4e-2

FS
type: SiteQuality
SIO_000300: 4.219e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.02e-2

QD
type: SiteQuality
SIO_000300: 9.4e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3342
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 9.81675392670157e-4
allele num: 3056
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.069451485349285e-5
allele num: 19726
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 322
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1360
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South Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.27e-2

ReadPosRankSum
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 2.992220227408737e-4
allele num: 3342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 26
allele frequency: 1.337448559670782e-3
allele num: 19440
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 3.041979314540661e-4
allele num: 9862
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Other
type: Population
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allele frequency: 3.205128205128205e-3
allele num: 312
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2014
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Latino
type: Population
allele count: 2
allele frequency: 6.821282401091405e-4
allele num: 2932
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1304
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BaseQRankSum
type: SiteQuality
SIO_000300: 4.8e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.43e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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allele num: 9670
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Latino
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African
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Other
type: Population
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ClippingRankSum
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MQRankSum
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FS
type: SiteQuality
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BaseQRankSum
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MQ
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DP
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InbreedingCoeff
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ReadPosRankSum
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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allele num: 286
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Latino
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South Asian
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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BaseQRankSum
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InbreedingCoeff
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FS
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MQRankSum
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DP
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QD
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ReadPosRankSum
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ClippingRankSum
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MQ
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 14772
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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Other
type: Population
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African
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allele frequency: 0.0e0
allele num: 2866
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9298
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.43e-2

QD
type: SiteQuality
SIO_000300: 1.499e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

DP
type: SiteQuality
SIO_000300: 5.10808e5

MQRankSum
type: SiteQuality
SIO_000300: -3.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

FS
type: SiteQuality
SIO_000300: 3.248e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

VQSLOD
type: SiteQuality
SIO_000300: -6.43e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

GenotypeQuality
all individuals: 151
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1076
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9202
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13864
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1824
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1356
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.71e-2

QD
type: SiteQuality
SIO_000300: 1.16e1

VQSLOD
type: SiteQuality
SIO_000300: 3.23e0

DP
type: SiteQuality
SIO_000300: 4.97451e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 5704
bin: 6.25e1
variant carriers: 4

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.25e1
variant carriers: 6

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 3

GenotypeQuality
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bin: 2.25e1
variant carriers: 5

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 9

GenotypeQuality
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bin: 5.75e1
variant carriers: 8

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 912
bin: 6.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1030
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 3.810975609756097e-3
allele num: 1312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 36
allele frequency: 3.11257132975964e-3
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 39
allele frequency: 4.383007417397168e-3
allele num: 8898
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 4.273504273504274e-3
allele num: 234
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.61619e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
SIO_000300: 1.334e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.49e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.049e0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-1

GenotypeQuality
all individuals: 71
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 157
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 303
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 294
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2344
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.030290541932825e-4
allele num: 9706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 962
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.648e0

DP
type: SiteQuality
SIO_000300: 4.3329e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.33e-1

QD
type: SiteQuality
SIO_000300: 1.017e1

GenotypeQuality
all individuals: 498
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 227
bin: 9.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2344
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 294
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.3329e5

QD
type: SiteQuality
SIO_000300: 1.017e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.648e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

GenotypeQuality
all individuals: 5848
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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
all individuals: 307
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 280
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 952
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2362
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.92e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 4.29804e5

QD
type: SiteQuality
SIO_000300: 7.96e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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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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variant carriers: 1

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 960
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.16767865483419e-4
allele num: 8564
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.148e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.74e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e-1

FS
type: SiteQuality
SIO_000300: 6.21e0

MQRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

DP
type: SiteQuality
SIO_000300: 4.29879e5

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.082e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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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
all individuals: 161
bin: 8.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
all individuals: 231
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 960
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9562
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2376
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.148e-1

DP
type: SiteQuality
SIO_000300: 4.29879e5

MQRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 6.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.74e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.082e1

GenotypeQuality
all individuals: 5455
bin: 6.25e1
variant carriers: 137

GenotypeQuality
all individuals: 185
bin: 8.25e1
variant carriers: 78

GenotypeQuality
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bin: 5.75e1
variant carriers: 165

GenotypeQuality
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bin: 4.75e1
variant carriers: 48

GenotypeQuality
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bin: 5.25e1
variant carriers: 72

GenotypeQuality
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bin: 2.75e1
variant carriers: 217

GenotypeQuality
all individuals: 131
bin: 3.75e1
variant carriers: 18

GenotypeQuality
all individuals: 394
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variant carriers: 107

GenotypeQuality
all individuals: 240
bin: 7.75e1
variant carriers: 29

GenotypeQuality
all individuals: 242
bin: 9.25e1
variant carriers: 193

GenotypeQuality
all individuals: 193
bin: 8.75e1
variant carriers: 143

GenotypeQuality
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bin: 1.25e1
variant carriers: 168

GenotypeQuality
all individuals: 7844
bin: 2.25e1
variant carriers: 238

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 16

Other
type: Population
allele count: 23
allele frequency: 1.036036036036036e-1
allele num: 222
num of homozygotes: 2

African
type: Population
allele count: 29
allele frequency: 1.211361737677527e-2
allele num: 2394
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 521
allele frequency: 5.578158458244111e-2
allele num: 9340
num of homozygotes: 11

East Asian
type: Population
allele count: 178
allele frequency: 2.045977011494253e-1
allele num: 870
num of homozygotes: 11

European (Finnish)
type: Population
allele count: 13
allele frequency: 5.284552845528456e-2
allele num: 246
num of homozygotes: 0

South Asian
type: Population
allele count: 968
allele frequency: 1.135617081182543e-1
allele num: 8524
num of homozygotes: 69

Latino
type: Population
allele count: 213
allele frequency: 2.356194690265487e-1
allele num: 904
num of homozygotes: 23

VQSLOD
type: SiteQuality
SIO_000300: 4.25e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.553e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

FS
type: SiteQuality
SIO_000300: 5.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.224e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

DP
type: SiteQuality
SIO_000300: 4.76055e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

GenotypeQuality
all individuals: 294
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2359
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
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variant carriers: 0

GenotypeQuality
all individuals: 3504
bin: 2.5e0
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GenotypeQuality
all individuals: 193
bin: 8.75e1
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GenotypeQuality
all individuals: 183
bin: 5.75e1
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GenotypeQuality
all individuals: 26918
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GenotypeQuality
all individuals: 7844
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 558
bin: 2.75e1
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GenotypeQuality
all individuals: 131
bin: 3.75e1
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GenotypeQuality
all individuals: 890
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GenotypeQuality
all individuals: 2382
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 242
bin: 9.25e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.448275862068965e-3
allele num: 870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9340
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.224e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.25e0

FS
type: SiteQuality
SIO_000300: 5.25e-1

QD
type: SiteQuality
SIO_000300: 1.553e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.76055e5

GenotypeQuality
all individuals: 147
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8180
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30775
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6143
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2427
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 9.75e1
variant carriers: 11

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2414
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8980
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.355013550135501e-3
allele num: 738
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 208
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 1.074755194650107e-3
allele num: 8374
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.16566e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.498e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e-1

FS
type: SiteQuality
SIO_000300: 5.064e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.35e-2

QD
type: SiteQuality
SIO_000300: 1.412e1

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.58e-1

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2566
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1991
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 9.25e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6987
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2388
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.160092807424594e-4
allele num: 8620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.09e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.45e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.26e0

DP
type: SiteQuality
SIO_000300: 4.07607e5

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 176
bin: 5.25e1
variant carriers: 154

GenotypeQuality
all individuals: 172
bin: 7.75e1
variant carriers: 68

GenotypeQuality
all individuals: 101
bin: 4.75e1
variant carriers: 70

GenotypeQuality
all individuals: 85
bin: 3.75e1
variant carriers: 39

GenotypeQuality
all individuals: 156
bin: 8.25e1
variant carriers: 122

GenotypeQuality
all individuals: 3862
bin: 2.25e1
variant carriers: 563

GenotypeQuality
all individuals: 3827
bin: 9.75e1
variant carriers: 3803

GenotypeQuality
all individuals: 23328
bin: 7.5e0
variant carriers: 745

GenotypeQuality
all individuals: 1131
bin: 1.25e1
variant carriers: 536

GenotypeQuality
all individuals: 5710
bin: 2.5e0
variant carriers: 6

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 33

GenotypeQuality
all individuals: 300
bin: 7.25e1
variant carriers: 137

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 213

GenotypeQuality
all individuals: 660
bin: 2.75e1
variant carriers: 533

Other
type: Population
allele count: 23
allele frequency: 1.185567010309278e-1
allele num: 194
num of homozygotes: 1

South Asian
type: Population
allele count: 744
allele frequency: 9.126594700686948e-2
allele num: 8152
num of homozygotes: 50

European (Non-Finnish)
type: Population
allele count: 1930
allele frequency: 2.277017461066541e-1
allele num: 8476
num of homozygotes: 165

Latino
type: Population
allele count: 162
allele frequency: 2.764505119453925e-1
allele num: 586
num of homozygotes: 21

African
type: Population
allele count: 692
allele frequency: 2.728706624605678e-1
allele num: 2536
num of homozygotes: 85

East Asian
type: Population
allele count: 21
allele frequency: 3.220858895705522e-2
allele num: 652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 29
allele frequency: 2.457627118644068e-1
allele num: 118
num of homozygotes: 3

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.160000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.658e1

MQRankSum
type: SiteQuality
SIO_000300: 2.85e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 4.94909e5

BaseQRankSum
type: SiteQuality
SIO_000300: -3.33e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.57e0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 649
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 9.75e1
variant carriers: 43

GenotypeQuality
all individuals: 29756
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 3115
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 27
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variant carriers: 1

GenotypeQuality
all individuals: 257
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6994
bin: 6.25e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2472
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7524
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 70
num of homozygotes: 0

South Asian
type: Population
allele count: 42
allele frequency: 5.248687828042989e-3
allele num: 8002
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.175e0

DP
type: SiteQuality
SIO_000300: 3.45426e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.66e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

FS
type: SiteQuality
SIO_000300: 1.795e0

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

QD
type: SiteQuality
SIO_000300: 1.283e1

MQ
type: SiteQuality
SIO_000300: 5.983e1

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29764
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
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variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
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GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 70
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variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2879
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1091
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 9.75e1
variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2474
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
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: 7480
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.251251251251251e-4
allele num: 7992
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.75e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.082e0

QD
type: SiteQuality
SIO_000300: 8.539999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.035e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.552e0

FS
type: SiteQuality
SIO_000300: 6.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.65e-2

MQ
type: SiteQuality
SIO_000300: 5.9e1

DP
type: SiteQuality
SIO_000300: 3.37801e5

GenotypeQuality
all individuals: 67
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7113
bin: 6.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2819
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 28924
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2529
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 256
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2472
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.25344697919278e-4
allele num: 7978
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7444
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.942e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-2

DP
type: SiteQuality
SIO_000300: 3.31681e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.72e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.41e0

MQRankSum
type: SiteQuality
SIO_000300: 2.54e0

QD
type: SiteQuality
SIO_000300: 1.005e1

FS
type: SiteQuality
SIO_000300: 4.198e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.66e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

GenotypeQuality
all individuals: 28306
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3034
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6995
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 254
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variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 9.75e1
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GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 7.75e1
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GenotypeQuality
all individuals: 68
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7960
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.350986219940557e-4
allele num: 7402
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.091e0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.235e1

FS
type: SiteQuality
SIO_000300: 2.632e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 3.28359e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.75e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 27313
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 169
bin: 7.75e1
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GenotypeQuality
all individuals: 124
bin: 2.75e1
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GenotypeQuality
all individuals: 1075
bin: 6.75e1
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GenotypeQuality
all individuals: 2994
bin: 2.5e0
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GenotypeQuality
all individuals: 66
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variant carriers: 0

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

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 9.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2446
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7944
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.20237e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.75e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.3e-1

QD
type: SiteQuality
SIO_000300: 1.267e1

MQ
type: SiteQuality
SIO_000300: 5.177e1

GenotypeQuality
all individuals: 6899
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 317
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 128
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1061
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 9.75e1
variant carriers: 11

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2436
num of homozygotes: 0

European (Finnish)
type: Population
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: 178
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.504787961696306e-3
allele num: 7310
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7936
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.929999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.729999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.88e0

ClippingRankSum
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SIO_000300: 2.5e-1

DP
type: SiteQuality
SIO_000300: 3.1549e5

QD
type: SiteQuality
SIO_000300: 1.267e1

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
all individuals: 119
bin: 3.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2410
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7246
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7924
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.84e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.537e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.54e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

VQSLOD
type: SiteQuality
SIO_000300: -2.137e0

QD
type: SiteQuality
SIO_000300: 8.369999999999999e0

DP
type: SiteQuality
SIO_000300: 3.0872e5

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7208
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34
num of homozygotes: 0

African
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allele count: 1
allele frequency: 4.205214465937763e-4
allele num: 2378
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7920
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.02451e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.037e0

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.14e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.91e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.75e-1

MQ
type: SiteQuality
SIO_000300: 5.499e1

QD
type: SiteQuality
SIO_000300: 1.445e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 364
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7054
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 3.731343283582089e-3
allele num: 536
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7904
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 6.751e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.829999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e0

MQ
type: SiteQuality
SIO_000300: 5.923e1

DP
type: SiteQuality
SIO_000300: 2.89913e5

VQSLOD
type: SiteQuality
SIO_000300: -1.042e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 1.042e1

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
all individuals: 38
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variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6964
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.270971021860702e-4
allele num: 7868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 360
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2262
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.741e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.511e0

FS
type: SiteQuality
SIO_000300: 7.574e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.67e-2

DP
type: SiteQuality
SIO_000300: 2.82386e5

QD
type: SiteQuality
SIO_000300: 1.092e1

MQRankSum
type: SiteQuality
SIO_000300: 1.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-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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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 500
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.460303300624443e-4
allele num: 2242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 350
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6912
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.67e-2

FS
type: SiteQuality
SIO_000300: 1.744e0

DP
type: SiteQuality
SIO_000300: 2.77912e5

VQSLOD
type: SiteQuality
SIO_000300: 8.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.09e-1

QD
type: SiteQuality
SIO_000300: 1.718e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e-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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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7850
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.416961130742049e-4
allele num: 6792
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2186
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 490
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 176
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.73616e5

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.975e1

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e-1

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

FS
type: SiteQuality
SIO_000300: 3.404e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.016e0

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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bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 1
allele frequency: 1.273885350318471e-4
allele num: 7850
num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
allele num: 344
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6776
num of homozygotes: 0

QD
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.141e0

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.580000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.64e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.73808e5

MQ
type: SiteQuality
SIO_000300: 5.92e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.36e-1

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

South Asian
type: Population
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allele frequency: 1.274859765425803e-4
allele num: 7844
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
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allele frequency: 1.482359916987845e-4
allele num: 6746
num of homozygotes: 0

Latino
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: -1.227e0

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.58e-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
all individuals: 38
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GenotypeQuality
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Other
type: Population
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allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.788e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.97e-2

FS
type: SiteQuality
SIO_000300: 2.947e0

DP
type: SiteQuality
SIO_000300: 2.72194e5

VQSLOD
type: SiteQuality
SIO_000300: -1.227e0

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.58e-1

QD
type: SiteQuality
SIO_000300: 1.087e1