3-69273788-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273788
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273788
    reference: chr 3
allele count: 2
allele frequency: 3.688131592535222e-5
allele num: 54228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.308C>G
  hgvsp: ENSP00000418962.1:p.Thr103Ser
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.473C>G
  hgvsp: ENSP00000437658.1:p.Thr158Ser
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.529C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.247C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.260C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.473C>G
  hgvsp: ENSP00000418373.1:p.Thr158Ser
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.635C>G
  hgvsp: ENSP00000381549.3:p.Thr212Ser
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6812
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30067
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2992
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8277
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1118
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1329
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr212Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

3-69273790-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273790
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273790
    reference: chr 3
allele count: 1
allele frequency: 1.84243496204584e-5
allele num: 54276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.258A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.471A>C
  hgvsp: ENSP00000437658.1:p.Lys157Asn
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.527A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.633A>C
  hgvsp: ENSP00000381549.3:p.Lys211Asn
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.245A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.471A>C
  hgvsp: ENSP00000418373.1:p.Lys157Asn
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.306A>C
  hgvsp: ENSP00000418962.1:p.Lys102Asn
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6904
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8443
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3022
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1315
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys211Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

3-69273791-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273791
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273791
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 54168
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.632A>G
  hgvsp: ENSP00000381549.3:p.Lys211Arg
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.526A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.257A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.244A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.305A>G
  hgvsp: ENSP00000418962.1:p.Lys102Arg
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.470A>G
  hgvsp: ENSP00000418373.1:p.Lys157Arg
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.470A>G
  hgvsp: ENSP00000437658.1:p.Lys157Arg
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30084
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1055
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1321
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8318
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6266
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Lys211Arg
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

3-69273792-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273792
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273792
    reference: chr 3
allele count: 1
allele frequency: 1.852537977028529e-5
allele num: 53980
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.631A>G
  hgvsp: ENSP00000381549.3:p.Lys211Glu
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.256A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.304A>G
  hgvsp: ENSP00000418962.1:p.Lys102Glu
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.469A>G
  hgvsp: ENSP00000418373.1:p.Lys157Glu
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.525A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.469A>G
  hgvsp: ENSP00000437658.1:p.Lys157Glu
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.243A>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30094
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7056
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33414
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3171
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8199
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys211Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD

3-69273797-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273797
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273797
    reference: chr 3
allele count: 1
allele frequency: 1.908324109766803e-5
allele num: 52402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.464C>T
  hgvsp: ENSP00000437658.1:p.Pro155Leu
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.464C>T
  hgvsp: ENSP00000418373.1:p.Pro155Leu
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.299C>T
  hgvsp: ENSP00000418962.1:p.Pro100Leu
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.251C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.238C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.626C>T
  hgvsp: ENSP00000381549.3:p.Pro209Leu
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.520C>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7852
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29958
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1276
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33569
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3887
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro209Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

3-69273798-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273798
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273798
    reference: chr 3
allele count: 1
allele frequency: 1.904399162064369e-5
allele num: 52510
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.463C>G
  hgvsp: ENSP00000437658.1:p.Pro155Ala
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.519C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.250C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.463C>G
  hgvsp: ENSP00000418373.1:p.Pro155Ala
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.237C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.625C>G
  hgvsp: ENSP00000381549.3:p.Pro209Ala
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.298C>G
  hgvsp: ENSP00000418962.1:p.Pro100Ala
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29997
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7829
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3727
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33894
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3868
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6970
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 754
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro209Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

3-69273806-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273806
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273806
    reference: chr 3
allele count: 1
allele frequency: 1.981532120635676e-5
allele num: 50466
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.455C>T
  hgvsp: ENSP00000437658.1:p.Pro152Leu
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.290C>T
  hgvsp: ENSP00000418962.1:p.Pro97Leu
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.511C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.242C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.617C>T
  hgvsp: ENSP00000381549.3:p.Pro206Leu
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.455C>T
  hgvsp: ENSP00000418373.1:p.Pro152Leu
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.229C>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29664
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4923
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4235
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1085
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5167
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro206Leu
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

3-69273813-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273813
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273813
    reference: chr 3
allele count: 2
allele frequency: 4.190061174893154e-5
allele num: 47732
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.448A>G
  hgvsp: ENSP00000437658.1:p.Thr150Ala
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.222A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.235A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.610A>G
  hgvsp: ENSP00000381549.3:p.Thr204Ala
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.448A>G
  hgvsp: ENSP00000418373.1:p.Thr150Ala
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.283A>G
  hgvsp: ENSP00000418962.1:p.Thr95Ala
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.504A>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28903
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7008
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9092
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 32025
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1406
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6266
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2437
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Thr204Ala
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/3-69273822-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273822
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273822
    reference: chr 3
allele count: 46
allele frequency: 1.005069043873449e-3
allele num: 45768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.226G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.213G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.495G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.439G>T
  hgvsp: ENSP00000437658.1:p.Asp147Tyr
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.601G>T
  hgvsp: ENSP00000381549.3:p.Asp201Tyr
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.439G>T
  hgvsp: ENSP00000418373.1:p.Asp147Tyr
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.274G>T
  hgvsp: ENSP00000418962.1:p.Asp92Tyr
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 28073
  bin: 7.5e0
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8743
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 9067
  bin: 1.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9042
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1191
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 845
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3243
  bin: 6.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp201Tyr
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

3-69273828-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273828
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273828
    reference: chr 3
allele count: 1
allele frequency: 2.29147571035747e-5
allele num: 43640
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.433A>G
  hgvsp: ENSP00000437658.1:p.Arg145Gly
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.595A>G
  hgvsp: ENSP00000381549.3:p.Arg199Gly
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.207A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.220A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.433A>G
  hgvsp: ENSP00000418373.1:p.Arg145Gly
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.268A>G
  hgvsp: ENSP00000418962.1:p.Arg90Gly
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.489A>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10786
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27138
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8695
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1377
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11160
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6259
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 8.25e1
  variant carriers: 1
hgvs: p.Arg199Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

3-69273830-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273830
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273830
    reference: chr 3
allele count: 1
allele frequency: 2.343896493530846e-5
allele num: 42664
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.487C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.266C>T
  hgvsp: ENSP00000418962.1:p.Ala89Val
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.205C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.431C>T
  hgvsp: ENSP00000437658.1:p.Ala144Val
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.593C>T
  hgvsp: ENSP00000381549.3:p.Ala198Val
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.431C>T
  hgvsp: ENSP00000418373.1:p.Ala144Val
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.218C>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8580
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26807
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11411
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6259
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29068
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala198Val
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

3-69273837-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273837
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273837
    reference: chr 3
allele count: 5
allele frequency: 1.250500200080032e-4
allele num: 39984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.259G>A
  hgvsp: ENSP00000418962.1:p.Glu87Lys
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.424G>A
  hgvsp: ENSP00000437658.1:p.Glu142Lys
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.480G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.211G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.586G>A
  hgvsp: ENSP00000381549.3:p.Glu196Lys
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.424G>A
  hgvsp: ENSP00000418023.1:p.Glu142Lys
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.424G>A
  hgvsp: ENSP00000418373.1:p.Glu142Lys
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.198G>A
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14075
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7801
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1111
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2533
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu196Lys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

3-69273839-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273839
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273839
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 39448
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.196A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.422A>G
  hgvsp: ENSP00000418373.1:p.Asp141Gly
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.584A>G
  hgvsp: ENSP00000381549.3:p.Asp195Gly
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.257A>G
  hgvsp: ENSP00000418962.1:p.Asp86Gly
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.209A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.478A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.422A>G
  hgvsp: ENSP00000437658.1:p.Asp141Gly
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.422A>G
  hgvsp: ENSP00000418023.1:p.Asp141Gly
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7603
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25056
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14796
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1931
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2509
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp195Gly
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum

3-69273848-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273848
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273848
    reference: chr 3
allele count: 3
allele frequency: 8.177952240758914e-5
allele num: 36684
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-7T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-7T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-7T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-7T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-7T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-7T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-7T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.420-7T>C
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22580
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18506
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6637
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23138
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1940
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1701
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 2.5e0
  variant carriers: 0
hgvs: c.582-7T>C
num of homozygotes: 1
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

3-69273849-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273849
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273849
    reference: chr 3
allele count: 2
allele frequency: 5.55000555000555e-5
allele num: 36036
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-8C>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-8C>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-8C>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-8C>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-8C>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-8C>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-8C>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.420-8C>A
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18946
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1808
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22162
  bin: 2.25e1
  variant carriers: 0
hgvs: c.582-8C>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

3-69273853-T-TATAAGTG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273853
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273860
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 34194
alternate allele: TATAAGTG
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-13_582-12insCACTTAT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.420-13_420-12insCACTTAT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-13_476-12insCACTTAT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-13_207-12insCACTTAT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-13_420-12insCACTTAT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-13_420-12insCACTTAT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-13_194-12insCACTTAT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-13_255-12insCACTTAT
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20536
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 912
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2443
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2642
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/3-69273856-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273856
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273856
    reference: chr 3
allele count: 1
allele frequency: 3.008423586040914e-5
allele num: 33240
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-15T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-15T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.420-15T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-15T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-15T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-15T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-15T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-15T>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22624
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2961
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

3-69273857-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273857
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273857
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 33272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-16T>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.420-16T>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-16T>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-16T>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-16T>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-16T>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-16T>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-16T>A
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22645
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19625
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2945
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17366
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

3-69273858-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273858
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273858
    reference: chr 3
allele count: 3
allele frequency: 9.311564963684897e-5
allele num: 32218
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-17A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-17A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-17A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.420-17A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-17A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-17A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-17A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-17A>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19054
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23400
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4943
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15698
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3215
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

3-69273862-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273862
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273862
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 29636
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-21C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-21C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-21C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-21C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.420-21C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-21C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-21C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-21C>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 25441
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17705
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2981
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6249
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1245
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD

3-69273865-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273865
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273865
    reference: chr 3
allele count: 1
allele frequency: 3.362927091740651e-5
allele num: 29736
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-24T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-24T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.420-24T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-24T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-24T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-24T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-24T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-24T>C
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25650
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17674
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4020
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

3-69273866-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273866
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273866
    reference: chr 3
allele count: 1
allele frequency: 3.578329635726043e-5
allele num: 27946
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-25A>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-25A>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-25A>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-25A>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-25A>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-25A>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-25A>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.420-25A>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25830
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9820
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2331
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

3-69273877-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69273877
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69273877
    reference: chr 3
allele count: 1
allele frequency: 3.875668552825362e-5
allele num: 25802
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-36C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-36C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-36C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-36C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-36C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-36C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.420-36C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-36C>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16963
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27274
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3415
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6235
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP

3-69277484-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69277484
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69277484
    reference: chr 3
allele count: 250
allele frequency: 1.618332470222682e-2
allele num: 15448
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-3643C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.419+47C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-3643C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-3643C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-3643C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-3643C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-3643C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-3643C>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 6.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 6.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 5.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 8.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 9.75e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 11
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum

3-69277507-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69277507
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69277507
    reference: chr 3
allele count: 1
allele frequency: 6.461617989144482e-5
allele num: 15476
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-3666A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-3666A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-3666A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-3666A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-3666A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.419+24A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-3666A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-3666A>C
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

3-69277550-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69277550
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69277550
    reference: chr 3
allele count: 1
allele frequency: 6.450780544445878e-5
allele num: 15502
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-3709T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-3709T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-3709T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-3709T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-3709T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.408-8T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-3709T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-3709T>C
  variant of: http://identifiers.org/hgnc/24886
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5977
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
hgvs: c.408-8T>C
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

3-69277551-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69277551
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69277551
    reference: chr 3
allele count: 1
allele frequency: 6.450780544445878e-5
allele num: 15502
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-3710A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-3710A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-3710A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-3710A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-3710A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-3710A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-3710A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.408-9A>C
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5978
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQ

3-69277702-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69277702
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69277702
    reference: chr 3
allele count: 1
allele frequency: 2.554931016862545e-4
allele num: 3914
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-3861G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.407+37G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-3861G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-3861G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-3861G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-3861G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-3861G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-3861G>A
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3204
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4169
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

3-69277721-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69277721
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69277721
    reference: chr 3
allele count: 1
allele frequency: 5.035246727089627e-4
allele num: 1986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-3880G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-3880G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.407+18G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-3880G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-3880G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-3880G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-3880G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-3880G>A
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3650
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4406
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4129
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/3-69277725-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69277725
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69277725
    reference: chr 3
allele count: 1
allele frequency: 5.834305717619603e-4
allele num: 1714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-3884G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-3884G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.407+14G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-3884G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-3884G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-3884G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-3884G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-3884G>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4551
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3197
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

3-69277733-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69277733
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69277733
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 1410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-3892G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-3892G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-3892G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-3892G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-3892G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-3892G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.407+6G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-3892G>A
  variant of: http://identifiers.org/hgnc/24886
canonical: false
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4813
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3095
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: c.407+6G>A
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

3-69277789-CGACCTGGGCAACACAGTGA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69277789
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69277770
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 224
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4981
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: CGACCTGGGCAACACAGTGA
site quality: MQ
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-69277790-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69277790
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69277790
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-3949C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-3949C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-3949C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-3949C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-3949C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-3949C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-3949C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.397-41C>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6304
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-69277796-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69277796
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69277796
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.476-3955C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.255-3955C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.194-3955C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.207-3955C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.397-47C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.582-3955C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.420-3955C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.420-3955C>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

3-69298329-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69298329
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69298329
    reference: chr 3
allele count: 1
allele frequency: 1.348326726532373e-5
allele num: 74166
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.419+48A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+865A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.193+48A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.254+48A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+865A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.475+48A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.419+48A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.581+48A>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3603
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19447
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7067
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1690
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15961
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4537
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3937
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2699
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5785
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/3-69298331-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69298331
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69298331
    reference: chr 3
allele count: 1
allele frequency: 1.353253220742665e-5
allele num: 73896
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.475+46G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.193+46G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+863G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.419+46G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.254+46G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.581+46G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+863G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.419+46G>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15949
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6621
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19447
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3480
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3934
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1916
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5635
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

3-69298337-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69298337
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69298337
    reference: chr 3
allele count: 1
allele frequency: 1.34603995046573e-5
allele num: 74292
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.419+40C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.254+40C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+857C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.475+40C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+857C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.193+40C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.581+40C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.419+40C>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15756
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19667
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3195
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4163
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5642
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1761
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2515
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2042
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19224
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

3-69298349-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69298349
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69298349
    reference: chr 3
allele count: 2
allele frequency: 2.65717170643567e-5
allele num: 75268
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.254+28A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+845A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.581+28A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.475+28A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+845A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.193+28A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.419+28A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.419+28A>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14114
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2021
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11344
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21336
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1091
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1747
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3883
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3227
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/3-69298358-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69298358
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69298358
    reference: chr 3
allele count: 1
allele frequency: 1.312163758037003e-5
allele num: 76210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.475+19G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.254+19G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.193+19G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+836G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.581+19G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.419+19G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.419+19G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+836G>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12068
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22056
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3528
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2196
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14592
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD

3-69298370-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69298370
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69298370
    reference: chr 3
allele count: 1
allele frequency: 1.276552287581699e-5
allele num: 78336
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.581+7C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.254+7C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.419+7C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.193+7C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.419+7C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+824C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+824C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.475+7C>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9790
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1339
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
hgvs: c.581+7C>T
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-69298380-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69298380
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69298380
    reference: chr 3
allele count: 1
allele frequency: 1.245547168871285e-5
allele num: 80286
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.578C>T
  hgvsp: ENSP00000381549.3:p.Thr193Ile
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.416C>T
  hgvsp: ENSP00000418023.1:p.Thr139Ile
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.190C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+814C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.416C>T
  hgvsp: ENSP00000418373.1:p.Thr139Ile
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.251C>T
  hgvsp: ENSP00000418962.1:p.Thr84Ile
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.472C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+814C>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18835
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17946
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8785
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 601
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 864
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2325
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr193Ile
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-69298387-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69298387
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69298387
    reference: chr 3
allele count: 12
allele frequency: 1.485552997103172e-4
allele num: 80778
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.571G>A
  hgvsp: ENSP00000381549.3:p.Asp191Asn
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.183G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.244G>A
  hgvsp: ENSP00000418962.1:p.Asp82Asn
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.409G>A
  hgvsp: ENSP00000418023.1:p.Asp137Asn
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+807G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.409G>A
  hgvsp: ENSP00000418373.1:p.Asp137Asn
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.465G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+807G>A
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17184
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4469
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9442
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3940
  bin: 9.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 741
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2634
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp191Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

3-69298401-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69298401
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69298400
    reference: chr 3
allele count: 672
allele frequency: 8.311071534579995e-3
allele num: 80856
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.397-3delT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+792delT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.453-3delT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.232-3delT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.171-3delT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+792delT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.559-3delT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.397-3delT
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14039
  bin: 2.25e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18264
  bin: 7.5e0
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 3.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 3.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 11786
  bin: 1.25e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 2.75e1
  variant carriers: 88
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 9.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 6.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 2050
  bin: 1.75e1
  variant carriers: 128
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 4.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 5.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1443
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 23589
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 5.75e1
  variant carriers: 6
hgvs: c.559-3delT
num of homozygotes: 19
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: TA
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/3-69298404-AAAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69298404
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69298401
    reference: chr 3
allele count: 1
allele frequency: 1.240540875821858e-5
allele num: 80610
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.397-8_397-6delGTT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.397-8_397-6delGTT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.171-8_171-6delGTT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.559-8_559-6delGTT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.453-8_453-6delGTT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+787_396+789delGTT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.232-8_232-6delGTT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+787_206+789delGTT
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 12328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18294
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3972
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1610
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3169
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 962
  bin: 5.25e1
  variant carriers: 0
hgvs: c.559-8_559-6delGTT
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: AAAC
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

3-69298406-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69298406
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69298406
    reference: chr 3
allele count: 2
allele frequency: 2.479851208927464e-5
allele num: 80650
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+788T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+788T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.397-7T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.171-7T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.559-7T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.232-7T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.397-7T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.453-7T>C
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12383
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2301
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3155
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1223
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1873
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14838
  bin: 6.25e1
  variant carriers: 0
hgvs: c.559-7T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS

3-69298409-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69298409
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69298409
    reference: chr 3
allele count: 2
allele frequency: 2.489172101359088e-5
allele num: 80348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.397-10T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+785T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.559-10T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.453-10T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.171-10T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+785T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.397-10T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.232-10T>C
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18177
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14102
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11133
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13149
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1839
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3500
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 852
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD

3-69298420-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69298420
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69298418
    reference: chr 3
allele count: 1
allele frequency: 1.254988579603926e-5
allele num: 79682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.171-23_171-22delCT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.559-23_559-22delCT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.397-23_397-22delCT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+772_206+773delCT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.453-23_453-22delCT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+772_396+773delCT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.232-23_232-22delCT
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.397-23_397-22delCT
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17790
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16323
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 835
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9904
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2160
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4651
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: CAG
site quality: DP
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

3-69298427-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69298427
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69298427
    reference: chr 3
allele count: 8
allele frequency: 1.011173466808231e-4
allele num: 79116
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.397-28C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.453-28C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.559-28C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.171-28C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+767C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+767C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.232-28C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.397-28C>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17612
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17007
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3974
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 2578
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1154
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8722
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1137
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5188
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 816
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: MQ
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: DP

3-69298435-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69298435
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69298435
    reference: chr 3
allele count: 15
allele frequency: 1.934784851924466e-4
allele num: 77528
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.397-36A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.397-36A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.453-36A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.171-36A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.559-36A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.232-36A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+759A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+759A>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16827
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7690
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17913
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3976
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2081
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21320
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 979
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

3-69299148-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299148
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299148
    reference: chr 3
allele count: 3
allele frequency: 2.490287877278613e-5
allele num: 120468
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.170+46C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+46C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.396+46C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.396+46C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.452+46C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.231+46C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.558+46C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+46C>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18760
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1977
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

3-69299148-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299148
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299148
    reference: chr 3
allele count: 1
allele frequency: 8.300959590928711e-6
allele num: 120468
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.396+46C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.396+46C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+46C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.452+46C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+46C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.170+46C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.231+46C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.558+46C>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18760
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/3-69299150-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299150
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299150
    reference: chr 3
allele count: 1
allele frequency: 8.300132802124834e-6
allele num: 120480
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.396+44T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.558+44T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.452+44T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.170+44T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+44T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.396+44T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.231+44T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+44T>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18759
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2190
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

3-69299160-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299160
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299160
    reference: chr 3
allele count: 1
allele frequency: 8.298066550493736e-6
allele num: 120510
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.558+34C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+34C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.396+34C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+34C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.452+34C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.170+34C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.396+34C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.231+34C>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18760
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-69299161-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299161
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299161
    reference: chr 3
allele count: 2
allele frequency: 1.659255326209597e-5
allele num: 120536
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.452+33C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.170+33C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+33C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.396+33C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.231+33C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+33C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.558+33C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.396+33C>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18761
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2864
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1131
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-69299164-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299164
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299164
    reference: chr 3
allele count: 1
allele frequency: 8.295863682367972e-6
allele num: 120542
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.558+30C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+30C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+30C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.396+30C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.452+30C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.170+30C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.396+30C>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.231+30C>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18761
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52599
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2944
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/3-69299171-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299171
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299171
    reference: chr 3
allele count: 1
allele frequency: 8.29242404139578e-6
allele num: 120592
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.452+23T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.170+23T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+23T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.231+23T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+23T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.396+23T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.558+23T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.396+23T>G
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18762
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52606
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1178
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
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: A
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

3-69299172-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299172
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299172
    reference: chr 3
allele count: 1
allele frequency: 8.292148993333113e-6
allele num: 120596
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+22C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.452+22C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.170+22C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.558+22C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.396+22C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.231+22C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+22C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.396+22C>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18763
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1180
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

3-69299173-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299173
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299173
    reference: chr 3
allele count: 1
allele frequency: 8.291873963515755e-6
allele num: 120600
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+21T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.170+21T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.452+21T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.396+21T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.558+21T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.396+21T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.231+21T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+21T>C
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3822
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4058
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18763
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3289
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1181
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/3-69299185-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299185
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299185
    reference: chr 3
allele count: 7494
allele frequency: 6.210119826971842e-2
allele num: 120674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.396+9G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.558+9G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.206+9G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.170+9G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.452+9G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.396+9G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.231+9G>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.396+9G>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 3.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 4.75e1
  variant carriers: 115
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 4.25e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 3663
  bin: 7.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 8.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3150
  bin: 6.25e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 1915
  bin: 2.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 3.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 5.75e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 3249
  bin: 8.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 6.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 5.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 9.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 22287
  bin: 9.75e1
  variant carriers: 6307
genotype depth: GenotypeDepth
  all individuals: 3677
  bin: 7.75e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3144
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 327
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

3-69299195-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299195
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299195
    reference: chr 3
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.169A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.557A>G
  hgvsp: ENSP00000381549.3:p.Gln186Arg
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.395A>G
  hgvsp: ENSP00000418373.1:p.Gln132Arg
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.205A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.395A>G
  hgvsp: ENSP00000418023.1:p.Gln132Arg
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.451A>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.395A>G
  hgvsp: ENSP00000437658.1:p.Gln132Arg
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.230A>G
  hgvsp: ENSP00000418962.1:p.Gln77Arg
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4060
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18601
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3947
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln186Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD

3-69299198-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299198
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299198
    reference: chr 3
allele count: 9
allele frequency: 7.455886007787258e-5
allele num: 120710
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.392T>C
  hgvsp: ENSP00000437658.1:p.Leu131Ser
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.448T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.392T>C
  hgvsp: ENSP00000418373.1:p.Leu131Ser
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.554T>C
  hgvsp: ENSP00000381549.3:p.Leu185Ser
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.202T>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.227T>C
  hgvsp: ENSP00000418962.1:p.Leu76Ser
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.392T>C
  hgvsp: ENSP00000418023.1:p.Leu131Ser
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.166T>C
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18601
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3947
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3386
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu185Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

3-69299206-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299206
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299206
    reference: chr 3
allele count: 2
allele frequency: 1.656561640658649e-5
allele num: 120732
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.546G>A
  hgvsp: ENST00000398540.3:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.384G>A
  hgvsp: ENST00000542259.1:c.384G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.440G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.384G>A
  hgvsp: ENST00000473029.1:c.384G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.219G>A
  hgvsp: ENST00000493880.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.384G>A
  hgvsp: ENST00000460709.1:c.384G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.194G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.158G>A
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3947
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala182Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

3-69299207-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299207
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299207
    reference: chr 3
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.383C>T
  hgvsp: ENSP00000437658.1:p.Ala128Val
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.545C>T
  hgvsp: ENSP00000381549.3:p.Ala182Val
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.383C>T
  hgvsp: ENSP00000418373.1:p.Ala128Val
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.439C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.193C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.218C>T
  hgvsp: ENSP00000418962.1:p.Ala73Val
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.383C>T
  hgvsp: ENSP00000418023.1:p.Ala128Val
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.157C>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3949
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18601
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3411
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala182Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

3-69299209-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299209
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299209
    reference: chr 3
allele count: 7
allele frequency: 5.797293492123963e-5
allele num: 120746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.216A>C
  hgvsp: ENST00000493880.1:c.216A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.543A>C
  hgvsp: ENST00000398540.3:c.543A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.191A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.381A>C
  hgvsp: ENST00000473029.1:c.381A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.381A>C
  hgvsp: ENST00000542259.1:c.381A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.437A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.381A>C
  hgvsp: ENST00000460709.1:c.381A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.155A>C
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2891
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18605
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3415
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala181Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/3-69299214-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299214
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299214
    reference: chr 3
allele count: 1
allele frequency: 8.281573498964803e-6
allele num: 120750
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.150T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.538T>G
  hgvsp: ENSP00000381549.3:p.Leu180Val
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.376T>G
  hgvsp: ENSP00000418373.1:p.Leu126Val
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.376T>G
  hgvsp: ENSP00000418023.1:p.Leu126Val
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.376T>G
  hgvsp: ENSP00000437658.1:p.Leu126Val
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.186T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.432T>G
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.211T>G
  hgvsp: ENSP00000418962.1:p.Leu71Val
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18599
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu180Val
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

3-69299216-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299216
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299216
    reference: chr 3
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.148A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.374A>C
  hgvsp: ENSP00000437658.1:p.Lys125Thr
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.209A>C
  hgvsp: ENSP00000418962.1:p.Lys70Thr
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.536A>C
  hgvsp: ENSP00000381549.3:p.Lys179Thr
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.430A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.374A>C
  hgvsp: ENSP00000418373.1:p.Lys125Thr
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.374A>C
  hgvsp: ENSP00000418023.1:p.Lys125Thr
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.184A>C
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18600
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 685
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3415
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Lys179Thr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

3-69299225-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299225
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299225
    reference: chr 3
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.527C>T
  hgvsp: ENSP00000381549.3:p.Thr176Ile
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.175C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.365C>T
  hgvsp: ENSP00000437658.1:p.Thr122Ile
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.365C>T
  hgvsp: ENSP00000418373.1:p.Thr122Ile
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.200C>T
  hgvsp: ENSP00000418962.1:p.Thr67Ile
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.139C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.365C>T
  hgvsp: ENSP00000418023.1:p.Thr122Ile
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.421C>T
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18600
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1235
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3420
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr176Ile
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

3-69299226-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299226
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299226
    reference: chr 3
allele count: 3
allele frequency: 2.484307457890989e-5
allele num: 120758
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.364A>C
  hgvsp: ENSP00000418023.1:p.Thr122Pro
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.526A>C
  hgvsp: ENSP00000381549.3:p.Thr176Pro
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.364A>C
  hgvsp: ENSP00000437658.1:p.Thr122Pro
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.420A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.364A>C
  hgvsp: ENSP00000418373.1:p.Thr122Pro
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.199A>C
  hgvsp: ENSP00000418962.1:p.Thr67Pro
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.174A>C
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.138A>C
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4084
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18601
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3492
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1235
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr176Pro
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

3-69299229-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299229
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299229
    reference: chr 3
allele count: 28
allele frequency: 2.318725363543012e-4
allele num: 120756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.417G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.361G>A
  hgvsp: ENSP00000418373.1:p.Glu121Lys
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.523G>A
  hgvsp: ENSP00000381549.3:p.Glu175Lys
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.171G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.196G>A
  hgvsp: ENSP00000418962.1:p.Glu66Lys
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.135G>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.361G>A
  hgvsp: ENSP00000418023.1:p.Glu121Lys
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.361G>A
  hgvsp: ENSP00000437658.1:p.Glu121Lys
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18610
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4081
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3950
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4062
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3945
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3528
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52494
  bin: 9.75e1
  variant carriers: 28
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu175Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD

3-69299230-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299230
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299230
    reference: chr 3
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.360C>T
  hgvsp: ENST00000460709.1:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.195C>T
  hgvsp: ENST00000493880.1:c.195C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.416C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.360C>T
  hgvsp: ENST00000542259.1:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.134C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.170C>T
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.522C>T
  hgvsp: ENST00000398540.3:c.522C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.360C>T
  hgvsp: ENST00000473029.1:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18600
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1234
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52485
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3420
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser174Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-69299230-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 69299230
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 69299230
    reference: chr 3
allele count: 3
allele frequency: 2.484307457890989e-5
allele num: 120758
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418373
  ensembl transcript: ENST00000473029
  gene symbol: FRMD4B
  hgvsc: ENST00000473029.1:c.360C>A
  hgvsp: ENSP00000418373.1:p.Ser120Arg
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000487751
  gene symbol: FRMD4B
  hgvsc: ENST00000487751.1:n.170C>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418962
  ensembl transcript: ENST00000493880
  gene symbol: FRMD4B
  hgvsc: ENST00000493880.1:c.195C>A
  hgvsp: ENSP00000418962.1:p.Ser65Arg
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000418023
  ensembl transcript: ENST00000460709
  gene symbol: FRMD4B
  hgvsc: ENST00000460709.1:c.360C>A
  hgvsp: ENSP00000418023.1:p.Ser120Arg
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000381549
  ensembl transcript: ENST00000398540
  gene symbol: FRMD4B
  hgvsc: ENST00000398540.3:c.522C>A
  hgvsp: ENSP00000381549.3:p.Ser174Arg
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000470070
  gene symbol: FRMD4B
  hgvsc: ENST00000470070.2:n.416C>A
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114541
  ensembl protein: ENSP00000437658
  ensembl transcript: ENST00000542259
  gene symbol: FRMD4B
  hgvsc: ENST00000542259.1:c.360C>A
  hgvsp: ENSP00000437658.1:p.Ser120Arg
  variant of: http://identifiers.org/hgnc/24886
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114541
  ensembl transcript: ENST00000483668
  gene symbol: FRMD4B
  hgvsc: ENST00000483668.1:n.134C>A
  variant of: http://identifiers.org/hgnc/24886
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3944
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18600
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3420
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1234
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser174Arg
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 138
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 762
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32924
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1032
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1072
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6267
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3938
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2974
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.095557418273261e-4
allele num: 9544
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5292
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28552
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.975e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.5e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 1.205842e6

QD
type: SiteQuality
SIO_000300: 1.295e1

FS
type: SiteQuality
SIO_000300: 1.041e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.59e-1

GenotypeQuality
all individuals: 455
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1027
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33221
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5306
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3922
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3000
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.502136303144918e-5
allele num: 28554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9568
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

DP
type: SiteQuality
SIO_000300: 1.204288e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.48e0

QD
type: SiteQuality
SIO_000300: 1.806e1

VQSLOD
type: SiteQuality
SIO_000300: -1.589e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.404e0

GenotypeQuality
all individuals: 98
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 372
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5300
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3906
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9564
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3462
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3000
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28474
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

FS
type: SiteQuality
SIO_000300: 1.871e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.78e-1

DP
type: SiteQuality
SIO_000300: 1.201854e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 5.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.567e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.56e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28384
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5292
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3444
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.04777870913663e-4
allele num: 9544
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2966
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.305e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.72e-1

FS
type: SiteQuality
SIO_000300: 1.114e0

VQSLOD
type: SiteQuality
SIO_000300: -5.602e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.54e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-3

DP
type: SiteQuality
SIO_000300: 1.200078e6

QD
type: SiteQuality
SIO_000300: 1.086e1

GenotypeQuality
all individuals: 138
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6265
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3718
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2850
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5146
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 442
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.646175162254795e-5
allele num: 27426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3354
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.57e0

DP
type: SiteQuality
SIO_000300: 1.18169e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 5.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

GenotypeQuality
all individuals: 1025
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1054
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 478
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variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6265
bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 600
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 968
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 698
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5132
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2866
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3716
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.054407423028258e-4
allele num: 9484
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 442
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.386e0

VQSLOD
type: SiteQuality
SIO_000300: -4.328e-1

QD
type: SiteQuality
SIO_000300: 6.89e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.8e-3

FS
type: SiteQuality
SIO_000300: 1.714e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

DP
type: SiteQuality
SIO_000300: 1.181948e6

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34076
bin: 2.25e1
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GenotypeQuality
all individuals: 919
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5659
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6266
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4972
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2714
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3276
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.829654782116582e-4
allele num: 3534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26178
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.21e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -8.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.55e-1

QD
type: SiteQuality
SIO_000300: 3.083e1

FS
type: SiteQuality
SIO_000300: 3.176e0

MQRankSum
type: SiteQuality
SIO_000300: 7.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.9e-2

DP
type: SiteQuality
SIO_000300: 1.154524e6

VQSLOD
type: SiteQuality
SIO_000300: -3.046e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
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GenotypeQuality
all individuals: 7247
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 953
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 600
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GenotypeQuality
all individuals: 223
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4726
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 8.143985666585227e-5
allele num: 24558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3136
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2400
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.55e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.129e0

QD
type: SiteQuality
SIO_000300: 5.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.025e0

DP
type: SiteQuality
SIO_000300: 1.117312e6

GenotypeQuality
all individuals: 457
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1325
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 94
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GenotypeQuality
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GenotypeQuality
all individuals: 6302
bin: 9.75e1
variant carriers: 49

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 841
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 750
bin: 7.75e1
variant carriers: 2

Latino
type: Population
allele count: 8
allele frequency: 3.633060853769301e-3
allele num: 2202
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 4.436557231588288e-4
allele num: 4508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3022
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 4.380201489268506e-4
allele num: 9132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3020
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 32
allele frequency: 1.36332651670075e-3
allele num: 23472
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.468e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.79e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.094789e6

QD
type: SiteQuality
SIO_000300: 1.205e1

GenotypeQuality
all individuals: 1226
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2276
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2698
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 55
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GenotypeQuality
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GenotypeQuality
all individuals: 747
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variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22158
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.110864252388358e-4
allele num: 9002
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1980
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4344
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2918
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

DP
type: SiteQuality
SIO_000300: 1.069416e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.21e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

FS
type: SiteQuality
SIO_000300: 8.574999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -1.334e0

QD
type: SiteQuality
SIO_000300: 6.15e0

GenotypeQuality
all individuals: 1185
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 736
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GenotypeQuality
all individuals: 2528
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GenotypeQuality
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GenotypeQuality
all individuals: 455
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GenotypeQuality
all individuals: 678
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GenotypeQuality
all individuals: 747
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variant carriers: 0

GenotypeQuality
all individuals: 696
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variant carriers: 0

GenotypeQuality
all individuals: 2237
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4250
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2754
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.630487127245786e-5
allele num: 21596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8944
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2870
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.062449e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.41e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

QD
type: SiteQuality
SIO_000300: 1.309e1

VQSLOD
type: SiteQuality
SIO_000300: 6.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 14521
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 3.25e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 454
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2720
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4026
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.264222503160556e-3
allele num: 1582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2502
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.499550134959512e-4
allele num: 20006
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.035638e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.313e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.83e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.383e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.304999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 600
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 777
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1099
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2456
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2704
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8760
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3988
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19660
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 354
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.87e-2

DP
type: SiteQuality
SIO_000300: 1.028477e6

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 1.112e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.093e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1608
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1262
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.476245654692932e-4
allele num: 8630
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17992
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3726
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2536
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 340
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.88e-1

QD
type: SiteQuality
SIO_000300: 2.171e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.199e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-2

DP
type: SiteQuality
SIO_000300: 9.96971e5

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 19473
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 2.73224043715847e-4
allele num: 3660
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 4.0e-4
allele num: 2500
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2124
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17634
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.65e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

FS
type: SiteQuality
SIO_000300: 3.692e0

QD
type: SiteQuality
SIO_000300: 8.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.28e-1

DP
type: SiteQuality
SIO_000300: 9.93142e5

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 600
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1928
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1056
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 3.816e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.373e0

FS
type: SiteQuality
SIO_000300: 9.336e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.668e0

QD
type: SiteQuality
SIO_000300: 1.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQRankSum
type: SiteQuality
SIO_000300: -1.369e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.954e0

DP
type: SiteQuality
SIO_000300: 9.72702e5

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3410
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2352
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.259389083625437e-5
allele num: 15976
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.109e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

QD
type: SiteQuality
SIO_000300: 9.01e0

DP
type: SiteQuality
SIO_000300: 9.59713e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.11e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.33e0

MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

FS
type: SiteQuality
SIO_000300: 8.529999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e0

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16002
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1794
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2348
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.09e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

DP
type: SiteQuality
SIO_000300: 9.59557e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -8.597e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

QD
type: SiteQuality
SIO_000300: 9.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

GenotypeQuality
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bin: 4.25e1
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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bin: 9.75e1
variant carriers: 7

GenotypeQuality
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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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8338
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.954142782699323e-4
allele num: 15352
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 926
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3286
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.38e0

QD
type: SiteQuality
SIO_000300: 1.508e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

FS
type: SiteQuality
SIO_000300: 8.62e-1

DP
type: SiteQuality
SIO_000300: 9.51714e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.41e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

GenotypeQuality
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bin: 2.25e1
variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 718
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GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3024
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1452
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2120
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8208
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 752
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

FS
type: SiteQuality
SIO_000300: 1.201e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.74e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.79e-1

DP
type: SiteQuality
SIO_000300: 9.27789e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.285e1

GenotypeQuality
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bin: 6.25e1
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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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 686
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.216841080554879e-4
allele num: 8218
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2128
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3028
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13854
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.67e-1

QD
type: SiteQuality
SIO_000300: 1.598e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.42e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

DP
type: SiteQuality
SIO_000300: 9.26533e5

VQSLOD
type: SiteQuality
SIO_000300: -1.717e0

MQRankSum
type: SiteQuality
SIO_000300: -1.212e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.63e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.81e0

GenotypeQuality
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bin: 8.25e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 644
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.538570417551309e-4
allele num: 2826
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 12774
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1292
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.452e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.98e-2

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 8.72e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.307e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-1

DP
type: SiteQuality
SIO_000300: 9.12929e5

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: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.724480893386844e-5
allele num: 11462
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8024
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1870
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1028
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2592
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.39e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.389e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.356e0

QD
type: SiteQuality
SIO_000300: 1.848e1

DP
type: SiteQuality
SIO_000300: 8.90917e5

GenotypeQuality
all individuals: 6002
bin: 9.75e1
variant carriers: 238

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 206
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4758
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 249
allele frequency: 3.267716535433071e-2
allele num: 7620
num of homozygotes: 11

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

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

Other
type: Population
allele count: 1
allele frequency: 5.050505050505051e-3
allele num: 198
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.05e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

DP
type: SiteQuality
SIO_000300: 4.50291e5

VQSLOD
type: SiteQuality
SIO_000300: 6.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.766e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.489e1

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 179
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GenotypeQuality
all individuals: 127
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4776
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.050505050505051e-3
allele num: 198
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.653e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.91e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

VQSLOD
type: SiteQuality
SIO_000300: 9.370000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.48e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.46e-1

QD
type: SiteQuality
SIO_000300: 9.039999999999999e0

DP
type: SiteQuality
SIO_000300: 4.49253e5

ClippingRankSum
type: SiteQuality
SIO_000300: -1.569e0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4796
num of homozygotes: 0

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.102e0

MQRankSum
type: SiteQuality
SIO_000300: 2.38e-1

FS
type: SiteQuality
SIO_000300: 5.017e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.68e-2

DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.105e1

VQSLOD
type: SiteQuality
SIO_000300: 3.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e0

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: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1646
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 204
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.050505050505051e-3
allele num: 198
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4796
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.891e1

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
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Other
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.01010101010101e-3
allele num: 990
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 540
num of homozygotes: 0

Latino
type: Population
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.85e-2

FS
type: SiteQuality
SIO_000300: 6.726e0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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South Asian
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African
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allele frequency: 9.803921568627451e-3
allele num: 102
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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
allele num: 564
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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FS
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 1.165501165501166e-3
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FS
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MQ
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ClippingRankSum
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QD
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VQSLOD
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ReadPosRankSum
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DP
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Other
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East Asian
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African
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South Asian
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European (Finnish)
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Latino
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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FS
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MQ
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QD
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Other
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Latino
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MQ
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DP
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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QD
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FS
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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European (Non-Finnish)
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African
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Latino
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South Asian
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East Asian
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QD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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DP
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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East Asian
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Latino
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European (Non-Finnish)
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Other
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InbreedingCoeff
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QD
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FS
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DP
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MQ
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
all individuals: 575
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5656
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7112
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.435697583787997e-5
allele num: 41056
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5948
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.54e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.722e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

DP
type: SiteQuality
SIO_000300: 1.109619e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.51e-1

FS
type: SiteQuality
SIO_000300: 6.101e0

QD
type: SiteQuality
SIO_000300: 4.68e0

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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bin: 9.75e1
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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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bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7268
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42346
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.686909581646424e-4
allele num: 5928
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4532
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6146
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.251e0

QD
type: SiteQuality
SIO_000300: 1.154e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.536e0

VQSLOD
type: SiteQuality
SIO_000300: 5.669999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.153274e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.268e0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7384
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4638
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.610305958132045e-4
allele num: 6210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43450
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11684
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

DP
type: SiteQuality
SIO_000300: 1.183867e6

VQSLOD
type: SiteQuality
SIO_000300: 4.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.023e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.23e-1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43738
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11728
num of homozygotes: 0

East Asian
type: Population
allele count: 11
allele frequency: 1.72090112640801e-3
allele num: 6392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6248
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.352813852813853e-4
allele num: 7392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4674
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

DP
type: SiteQuality
SIO_000300: 1.182154e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.19e1

FS
type: SiteQuality
SIO_000300: 1.103e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.61e0

MQRankSum
type: SiteQuality
SIO_000300: -1.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e-1

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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variant carriers: 613

GenotypeQuality
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variant carriers: 12

GenotypeQuality
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variant carriers: 11

GenotypeQuality
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bin: 3.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6360
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.507742045261188e-5
allele num: 11754
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4664
num of homozygotes: 0

African
type: Population
allele count: 633
allele frequency: 8.342119135477069e-2
allele num: 7588
num of homozygotes: 19

Other
type: Population
allele count: 2
allele frequency: 3.355704697986577e-3
allele num: 596
num of homozygotes: 0

Latino
type: Population
allele count: 24
allele frequency: 3.841229193341869e-3
allele num: 6248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 2.749392842413967e-4
allele num: 43646
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.006e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.52e0

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.05e-2

QD
type: SiteQuality
SIO_000300: 1.302e1

DP
type: SiteQuality
SIO_000300: 1.160145e6

FS
type: SiteQuality
SIO_000300: 5.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 8.510638297872341e-5
allele num: 11750
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43612
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7450
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4648
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.67e-1

DP
type: SiteQuality
SIO_000300: 1.134624e6

MQ
type: SiteQuality
SIO_000300: 5.944e1

MQRankSum
type: SiteQuality
SIO_000300: -3.07e-1

FS
type: SiteQuality
SIO_000300: 8.648e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.24e-1

QD
type: SiteQuality
SIO_000300: 6.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.294e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.26e-1

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.581271761040865e-5
allele num: 43656
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6198
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6364
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11746
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4644
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.11e-1

DP
type: SiteQuality
SIO_000300: 1.134906e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.67e0

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.08e-1

QD
type: SiteQuality
SIO_000300: 1.365e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.59e-1

FS
type: SiteQuality
SIO_000300: 2.596e0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.600027600165601e-5
allele num: 43478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6158
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11716
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7428
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4628
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.12142e6

FS
type: SiteQuality
SIO_000300: 6.488e0

VQSLOD
type: SiteQuality
SIO_000300: 2.45e-1

QD
type: SiteQuality
SIO_000300: 1.142e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11674
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 4586
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6302
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.320185614849188e-5
allele num: 43100
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.082516e6

QD
type: SiteQuality
SIO_000300: 1.168e1

FS
type: SiteQuality
SIO_000300: 8.768000000000001e0

ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.01e-1

InbreedingCoeff
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BaseQRankSum
type: SiteQuality
SIO_000300: -7.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.36e0

MQ
type: SiteQuality
SIO_000300: 6.042e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 484
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23827
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4370
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 707
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1561
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 8
allele frequency: 6.869311351537008e-4
allele num: 11646
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42768
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5970
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4556
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7328
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-2

VQSLOD
type: SiteQuality
SIO_000300: -7.292999999999999e-1

FS
type: SiteQuality
SIO_000300: 8.724e0

QD
type: SiteQuality
SIO_000300: 1.736e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.34e-1

DP
type: SiteQuality
SIO_000300: 1.063171e6

GenotypeQuality
all individuals: 306
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1126
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4502
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4038
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 504
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2226
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5571
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5870
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 5.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3554
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6154
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5716
num of homozygotes: 0

South Asian
type: Population
allele count: 15
allele frequency: 1.300502861106294e-3
allele num: 11534
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41862
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7220
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.03095e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.28e0

QD
type: SiteQuality
SIO_000300: 1.243e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.4e-3

GenotypeQuality
all individuals: 351
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 52588
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 215
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 695
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.105751618024179e-5
allele num: 16378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003453972067878e-5
allele num: 66590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

QD
type: SiteQuality
SIO_000300: 1.528e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

FS
type: SiteQuality
SIO_000300: 6.027e0

DP
type: SiteQuality
SIO_000300: 4.964581e6

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.69e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

GenotypeQuality
all individuals: 21
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 52588
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 249
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variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 7.25e1
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GenotypeQuality
all individuals: 608
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1977
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501726986033939e-5
allele num: 66590
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.027e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

DP
type: SiteQuality
SIO_000300: 4.964581e6

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.15e-1

QD
type: SiteQuality
SIO_000300: 1.528e1

MQ
type: SiteQuality
SIO_000300: 5.98e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.69e0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 245
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variant carriers: 0

GenotypeQuality
all individuals: 614
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 703
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variant carriers: 0

GenotypeQuality
all individuals: 52592
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 359
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variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501862309263487e-5
allele num: 66584
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

FS
type: SiteQuality
SIO_000300: 1.569e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.85e-1

QD
type: SiteQuality
SIO_000300: 1.009e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.55e-1

DP
type: SiteQuality
SIO_000300: 4.965433e6

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 4.17e-1

GenotypeQuality
all individuals: 178
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
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GenotypeQuality
all individuals: 1126
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
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variant carriers: 0

GenotypeQuality
all individuals: 745
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variant carriers: 0

GenotypeQuality
all individuals: 52599
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2824
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 503
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variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.093845216331505e-5
allele num: 16410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9794
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

QD
type: SiteQuality
SIO_000300: 1.85e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.25e-1

DP
type: SiteQuality
SIO_000300: 4.972066e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.47e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.084e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.023e0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 52601
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variant carriers: 2

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
all individuals: 93
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variant carriers: 0

GenotypeQuality
all individuals: 182
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GenotypeQuality
all individuals: 599
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GenotypeQuality
all individuals: 509
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variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66612
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.041649652919559e-4
allele num: 9796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

FS
type: SiteQuality
SIO_000300: 1.859e0

MQ
type: SiteQuality
SIO_000300: 5.932e1

DP
type: SiteQuality
SIO_000300: 4.972563e6

MQRankSum
type: SiteQuality
SIO_000300: 5.570000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.41e-1

QD
type: SiteQuality
SIO_000300: 1.395e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.28e-1

GenotypeQuality
all individuals: 1133
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
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variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
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GenotypeQuality
all individuals: 147
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
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GenotypeQuality
all individuals: 87
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GenotypeQuality
all individuals: 754
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variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.281e0

MQRankSum
type: SiteQuality
SIO_000300: -2.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 6.269e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.09e-1

DP
type: SiteQuality
SIO_000300: 4.973831e6

QD
type: SiteQuality
SIO_000300: 1.283e1

GenotypeQuality
all individuals: 65
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 773
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variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
all individuals: 110
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GenotypeQuality
all individuals: 3256
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GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 26
bin: 4.25e1
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GenotypeQuality
all individuals: 538
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GenotypeQuality
all individuals: 672
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500600240096038e-5
allele num: 66640
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.978207e6

VQSLOD
type: SiteQuality
SIO_000300: 7.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

FS
type: SiteQuality
SIO_000300: 4.376e0

MQRankSum
type: SiteQuality
SIO_000300: -2.53e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

QD
type: SiteQuality
SIO_000300: 1.435e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

GenotypeQuality
all individuals: 3253
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 7.5e0
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GenotypeQuality
all individuals: 56
bin: 3.75e1
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GenotypeQuality
all individuals: 52606
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 538
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GenotypeQuality
all individuals: 673
bin: 8.25e1
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 775
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variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.375e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.66e-1

QD
type: SiteQuality
SIO_000300: 1.386e1

MQ
type: SiteQuality
SIO_000300: 5.898e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.625e0

MQRankSum
type: SiteQuality
SIO_000300: 2.02e0

FS
type: SiteQuality
SIO_000300: 1.098e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.631e0

DP
type: SiteQuality
SIO_000300: 4.978488e6

GenotypeQuality
all individuals: 50
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 609
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GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500600240096038e-5
allele num: 66640
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.413e0

QD
type: SiteQuality
SIO_000300: 7.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.17e0

VQSLOD
type: SiteQuality
SIO_000300: -2.989e0

MQRankSum
type: SiteQuality
SIO_000300: -2.23e-1

DP
type: SiteQuality
SIO_000300: 4.978857e6

MQ
type: SiteQuality
SIO_000300: 5.987e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
all individuals: 14
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variant carriers: 1

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

Other
type: Population
allele count: 68
allele frequency: 7.572383073496659e-2
allele num: 898
num of homozygotes: 8

African
type: Population
allele count: 134
allele frequency: 1.367626046131864e-2
allele num: 9798
num of homozygotes: 2

South Asian
type: Population
allele count: 372
allele frequency: 2.256733802475127e-2
allele num: 16484
num of homozygotes: 8

European (Non-Finnish)
type: Population
allele count: 6097
allele frequency: 9.14367126574685e-2
allele num: 66680
num of homozygotes: 285

Latino
type: Population
allele count: 558
allele frequency: 4.820317899101589e-2
allele num: 11576
num of homozygotes: 16

European (Finnish)
type: Population
allele count: 264
allele frequency: 3.991533111581494e-2
allele num: 6614
num of homozygotes: 8

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.16e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.32e-1

DP
type: SiteQuality
SIO_000300: 5.547449e6

MQ
type: SiteQuality
SIO_000300: 5.961e1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.8e0

FS
type: SiteQuality
SIO_000300: 6.33e-1

QD
type: SiteQuality
SIO_000300: 1.421e1

GenotypeQuality
all individuals: 740
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 52478
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.06e0

MQRankSum
type: SiteQuality
SIO_000300: -1.093e0

MQ
type: SiteQuality
SIO_000300: 5.902e1

VQSLOD
type: SiteQuality
SIO_000300: -9.429999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 1.214e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.05e-1

DP
type: SiteQuality
SIO_000300: 5.025535e6

QD
type: SiteQuality
SIO_000300: 1.42e1

GenotypeQuality
all individuals: 427
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 811
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.349365798074905e-4
allele num: 66698
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 5.026006e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.16e0

MQRankSum
type: SiteQuality
SIO_000300: -1.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 1.437e1

FS
type: SiteQuality
SIO_000300: 5.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.909e1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.26e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 427
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

DP
type: SiteQuality
SIO_000300: 5.026055e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

QD
type: SiteQuality
SIO_000300: 1.061e1

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

FS
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.53e-1

ReadPosRankSum
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QD
type: SiteQuality
SIO_000300: 1.137e1

VQSLOD
type: SiteQuality
SIO_000300: -1.626e0

DP
type: SiteQuality
SIO_000300: 5.026232e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.932e1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

Latino
type: Population
allele count: 7
allele frequency: 6.046993780234969e-4
allele num: 11576
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
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allele num: 898
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8626
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

Other
type: Population
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allele num: 898
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.020199959192002e-4
allele num: 9802
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South Asian
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allele count: 0
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.579e0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 1.628e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.12e-1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.976e0

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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52483
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 742
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.39e-1

FS
type: SiteQuality
SIO_000300: 4.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.064e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
type: SiteQuality
SIO_000300: 7.44e-1

QD
type: SiteQuality
SIO_000300: 1.055e1

DP
type: SiteQuality
SIO_000300: 5.026482e6

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52484
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 815
bin: 7.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.964e1

DP
type: SiteQuality
SIO_000300: 5.026605e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.026e0

FS
type: SiteQuality
SIO_000300: 3.521e0

QD
type: SiteQuality
SIO_000300: 1.451e1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.852e0

GenotypeQuality
all individuals: 742
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3419
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 815
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 684
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52484
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.060599877576005e-4
allele num: 9802
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.19e-1

DP
type: SiteQuality
SIO_000300: 5.026985e6

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.36e-2

FS
type: SiteQuality
SIO_000300: 2.44e0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.6e-1

QD
type: SiteQuality
SIO_000300: 1.711e1

VQSLOD
type: SiteQuality
SIO_000300: 3.0e-1

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1234
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 742
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3414
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 1.150817686250757e-3
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.049003446725611e-4
allele num: 66730
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.58e0

DP
type: SiteQuality
SIO_000300: 5.029493e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.21e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

QD
type: SiteQuality
SIO_000300: 1.191e1

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 742
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 683
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 566
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.54e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.44e-1

DP
type: SiteQuality
SIO_000300: 5.027184e6

MQ
type: SiteQuality
SIO_000300: 5.932e1

MQRankSum
type: SiteQuality
SIO_000300: 5.22e-1

QD
type: SiteQuality
SIO_000300: 1.157e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.9e-2