11-8008976-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8008976
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8008976
    reference: chr 11
allele count: 2
allele frequency: 1.777904206521353e-5
allele num: 112492
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000396929
  ensembl transcript: ENST00000449102
  gene symbol: EIF3F
  hgvsc: ENST00000449102.2:c.-300T>C
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000310040
  ensembl transcript: ENST00000309828
  gene symbol: EIF3F
  hgvsc: ENST00000309828.4:c.77T>C
  hgvsp: ENSP00000310040.4:p.Val26Ala
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000442283
  ensembl transcript: ENST00000537635
  gene symbol: EIF3F
  hgvsc: ENST00000537635.1:c.122T>C
  hgvsp: ENSP00000442283.1:p.Val41Ala
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000432489
  ensembl transcript: ENST00000531329
  gene symbol: EIF3F
  hgvsc: ENST00000531329.1:c.77T>C
  hgvsp: ENSP00000432489.1:p.Val26Ala
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000431800
  ensembl transcript: ENST00000533626
  gene symbol: EIF3F
  hgvsc: ENST00000533626.1:c.77T>C
  hgvsp: ENSP00000431800.1:p.Val26Ala
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175390
  ensembl transcript: ENST00000528653
  gene symbol: EIF3F
  hgvsc: ENST00000528653.1:n.74T>C
  variant of: http://identifiers.org/hgnc/3275
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12087
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26991
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1691
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2275
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8832
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val26Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-8008978-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8008978
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8008978
    reference: chr 11
allele count: 1
allele frequency: 8.897272096375252e-6
allele num: 112394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000310040
  ensembl transcript: ENST00000309828
  gene symbol: EIF3F
  hgvsc: ENST00000309828.4:c.79C>T
  hgvsp: ENSP00000310040.4:p.Pro27Ser
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000442283
  ensembl transcript: ENST00000537635
  gene symbol: EIF3F
  hgvsc: ENST00000537635.1:c.124C>T
  hgvsp: ENSP00000442283.1:p.Pro42Ser
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000396929
  ensembl transcript: ENST00000449102
  gene symbol: EIF3F
  hgvsc: ENST00000449102.2:c.-298C>T
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000432489
  ensembl transcript: ENST00000531329
  gene symbol: EIF3F
  hgvsc: ENST00000531329.1:c.79C>T
  hgvsp: ENSP00000432489.1:p.Pro27Ser
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175390
  ensembl transcript: ENST00000528653
  gene symbol: EIF3F
  hgvsc: ENST00000528653.1:n.76C>T
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000431800
  ensembl transcript: ENST00000533626
  gene symbol: EIF3F
  hgvsc: ENST00000533626.1:c.79C>T
  hgvsp: ENSP00000431800.1:p.Pro27Ser
  variant of: http://identifiers.org/hgnc/3275
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2248
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2059
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38275
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2269
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
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genotype quality: GenotypeQuality
  all individuals: 1531
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro27Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

11-8008981-G-GCGCCAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8008981
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8008987
    reference: chr 11
allele count: 1
allele frequency: 8.902658333778466e-6
allele num: 112326
alternate allele: GCGCCAA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175390
  ensembl transcript: ENST00000528653
  gene symbol: EIF3F
  hgvsc: ENST00000528653.1:n.85_90dupACGCCA
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000396929
  ensembl transcript: ENST00000449102
  gene symbol: EIF3F
  hgvsc: ENST00000449102.2:c.-289_-284dupACGCCA
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000442283
  ensembl transcript: ENST00000537635
  gene symbol: EIF3F
  hgvsc: ENST00000537635.1:c.133_138dupACGCCA
  hgvsp: ENSP00000442283.1:p.Thr45_Pro46dup
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000431800
  ensembl transcript: ENST00000533626
  gene symbol: EIF3F
  hgvsc: ENST00000533626.1:c.88_93dupACGCCA
  hgvsp: ENSP00000431800.1:p.Thr30_Pro31dup
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000432489
  ensembl transcript: ENST00000531329
  gene symbol: EIF3F
  hgvsc: ENST00000531329.1:c.88_93dupACGCCA
  hgvsp: ENSP00000432489.1:p.Thr30_Pro31dup
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000310040
  ensembl transcript: ENST00000309828
  gene symbol: EIF3F
  hgvsc: ENST00000309828.4:c.88_93dupACGCCA
  hgvsp: ENSP00000310040.4:p.Thr30_Pro31dup
  variant of: http://identifiers.org/hgnc/3275
canonical: true
consequence: inframe insertion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1059
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26824
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38165
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 910
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2051
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2260
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr30_Pro31dup
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/11-8008987-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8008987
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8008987
    reference: chr 11
allele count: 2
allele frequency: 1.784153151706542e-5
allele num: 112098
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000396929
  ensembl transcript: ENST00000449102
  gene symbol: EIF3F
  hgvsc: ENST00000449102.2:c.-289A>C
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000442283
  ensembl transcript: ENST00000537635
  gene symbol: EIF3F
  hgvsc: ENST00000537635.1:c.133A>C
  hgvsp: ENSP00000442283.1:p.Thr45Pro
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000431800
  ensembl transcript: ENST00000533626
  gene symbol: EIF3F
  hgvsc: ENST00000533626.1:c.88A>C
  hgvsp: ENSP00000431800.1:p.Thr30Pro
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000310040
  ensembl transcript: ENST00000309828
  gene symbol: EIF3F
  hgvsc: ENST00000309828.4:c.88A>C
  hgvsp: ENSP00000310040.4:p.Thr30Pro
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175390
  ensembl transcript: ENST00000528653
  gene symbol: EIF3F
  hgvsc: ENST00000528653.1:n.85A>C
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000432489
  ensembl transcript: ENST00000531329
  gene symbol: EIF3F
  hgvsc: ENST00000531329.1:c.88A>C
  hgvsp: ENSP00000432489.1:p.Thr30Pro
  variant of: http://identifiers.org/hgnc/3275
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8627
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr30Pro
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

11-8008987-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8008987
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8008987
    reference: chr 11
allele count: 13
allele frequency: 1.159699548609253e-4
allele num: 112098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000310040
  ensembl transcript: ENST00000309828
  gene symbol: EIF3F
  hgvsc: ENST00000309828.4:c.88A>G
  hgvsp: ENSP00000310040.4:p.Thr30Ala
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000431800
  ensembl transcript: ENST00000533626
  gene symbol: EIF3F
  hgvsc: ENST00000533626.1:c.88A>G
  hgvsp: ENSP00000431800.1:p.Thr30Ala
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000442283
  ensembl transcript: ENST00000537635
  gene symbol: EIF3F
  hgvsc: ENST00000537635.1:c.133A>G
  hgvsp: ENSP00000442283.1:p.Thr45Ala
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000396929
  ensembl transcript: ENST00000449102
  gene symbol: EIF3F
  hgvsc: ENST00000449102.2:c.-289A>G
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000432489
  ensembl transcript: ENST00000531329
  gene symbol: EIF3F
  hgvsc: ENST00000531329.1:c.88A>G
  hgvsp: ENSP00000432489.1:p.Thr30Ala
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175390
  ensembl transcript: ENST00000528653
  gene symbol: EIF3F
  hgvsc: ENST00000528653.1:n.85A>G
  variant of: http://identifiers.org/hgnc/3275
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26559
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 8627
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 902
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1982
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr30Ala
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

11-8008992-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8008992
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8008992
    reference: chr 11
allele count: 1
allele frequency: 8.948545861297538e-6
allele num: 111750
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000442283
  ensembl transcript: ENST00000537635
  gene symbol: EIF3F
  hgvsc: ENST00000537635.1:c.138A>G
  hgvsp: ENST00000537635.1:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000310040
  ensembl transcript: ENST00000309828
  gene symbol: EIF3F
  hgvsc: ENST00000309828.4:c.93A>G
  hgvsp: ENST00000309828.4:c.93A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000396929
  ensembl transcript: ENST00000449102
  gene symbol: EIF3F
  hgvsc: ENST00000449102.2:c.-284A>G
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000432489
  ensembl transcript: ENST00000531329
  gene symbol: EIF3F
  hgvsc: ENST00000531329.1:c.93A>G
  hgvsp: ENST00000531329.1:c.93A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175390
  ensembl transcript: ENST00000528653
  gene symbol: EIF3F
  hgvsc: ENST00000528653.1:n.90A>G
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000431800
  ensembl transcript: ENST00000533626
  gene symbol: EIF3F
  hgvsc: ENST00000533626.1:c.93A>G
  hgvsp: ENST00000533626.1:c.93A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3275
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26287
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1651
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8455
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2225
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36853
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro31Pro
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-8008998-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8008998
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8008998
    reference: chr 11
allele count: 1
allele frequency: 8.981982143819498e-6
allele num: 111334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175390
  ensembl transcript: ENST00000528653
  gene symbol: EIF3F
  hgvsc: ENST00000528653.1:n.96G>C
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000432489
  ensembl transcript: ENST00000531329
  gene symbol: EIF3F
  hgvsc: ENST00000531329.1:c.99G>C
  hgvsp: ENST00000531329.1:c.99G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000442283
  ensembl transcript: ENST00000537635
  gene symbol: EIF3F
  hgvsc: ENST00000537635.1:c.144G>C
  hgvsp: ENST00000537635.1:c.144G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000396929
  ensembl transcript: ENST00000449102
  gene symbol: EIF3F
  hgvsc: ENST00000449102.2:c.-278G>C
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000310040
  ensembl transcript: ENST00000309828
  gene symbol: EIF3F
  hgvsc: ENST00000309828.4:c.99G>C
  hgvsp: ENST00000309828.4:c.99G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000431800
  ensembl transcript: ENST00000533626
  gene symbol: EIF3F
  hgvsc: ENST00000533626.1:c.99G>C
  hgvsp: ENST00000533626.1:c.99G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3275
canonical: true
consequence: synonymous
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1985
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8242
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2601
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1638
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1617
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro33Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

11-8008998-GGCTGCGGCTCCGGTTCCC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8008998
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8008980
    reference: chr 11
allele count: 1
allele frequency: 8.981982143819498e-6
allele num: 111334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000442283
  ensembl transcript: ENST00000537635
  gene symbol: EIF3F
  hgvsp: ENSP00000442283.1:p.Val53_Pro58del
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000432489
  ensembl transcript: ENST00000531329
  gene symbol: EIF3F
  hgvsp: ENSP00000432489.1:p.Val38_Pro43del
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000310040
  ensembl transcript: ENST00000309828
  gene symbol: EIF3F
  hgvsp: ENSP00000310040.4:p.Val38_Pro43del
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175390
  ensembl transcript: ENST00000528653
  gene symbol: EIF3F
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000396929
  ensembl transcript: ENST00000449102
  gene symbol: EIF3F
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000431800
  ensembl transcript: ENST00000533626
  gene symbol: EIF3F
  hgvsp: ENSP00000431800.1:p.Val38_Pro43del
  variant of: http://identifiers.org/hgnc/3275
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 10113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1814
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 513
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 878
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2184
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1638
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2601
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8242
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val38_Pro43del
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: GGCTGCGGCTCCGGTTCCC
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

11-8009003-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8009003
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8009003
    reference: chr 11
allele count: 3
allele frequency: 2.703871944624703e-5
allele num: 110952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000310040
  ensembl transcript: ENST00000309828
  gene symbol: EIF3F
  hgvsc: ENST00000309828.4:c.104C>T
  hgvsp: ENSP00000310040.4:p.Ala35Val
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000431800
  ensembl transcript: ENST00000533626
  gene symbol: EIF3F
  hgvsc: ENST00000533626.1:c.104C>T
  hgvsp: ENSP00000431800.1:p.Ala35Val
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000432489
  ensembl transcript: ENST00000531329
  gene symbol: EIF3F
  hgvsc: ENST00000531329.1:c.104C>T
  hgvsp: ENSP00000432489.1:p.Ala35Val
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000442283
  ensembl transcript: ENST00000537635
  gene symbol: EIF3F
  hgvsc: ENST00000537635.1:c.149C>T
  hgvsp: ENSP00000442283.1:p.Ala50Val
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000396929
  ensembl transcript: ENST00000449102
  gene symbol: EIF3F
  hgvsc: ENST00000449102.2:c.-273C>T
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175390
  ensembl transcript: ENST00000528653
  gene symbol: EIF3F
  hgvsc: ENST00000528653.1:n.101C>T
  variant of: http://identifiers.org/hgnc/3275
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12359
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8148
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1957
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1628
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala35Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

11-8009004-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8009004
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8009004
    reference: chr 11
allele count: 2
allele frequency: 1.801931670751045e-5
allele num: 110992
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000310040
  ensembl transcript: ENST00000309828
  gene symbol: EIF3F
  hgvsc: ENST00000309828.4:c.105G>A
  hgvsp: ENST00000309828.4:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000396929
  ensembl transcript: ENST00000449102
  gene symbol: EIF3F
  hgvsc: ENST00000449102.2:c.-272G>A
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000442283
  ensembl transcript: ENST00000537635
  gene symbol: EIF3F
  hgvsc: ENST00000537635.1:c.150G>A
  hgvsp: ENST00000537635.1:c.150G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175390
  ensembl transcript: ENST00000528653
  gene symbol: EIF3F
  hgvsc: ENST00000528653.1:n.102G>A
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000431800
  ensembl transcript: ENST00000533626
  gene symbol: EIF3F
  hgvsc: ENST00000533626.1:c.105G>A
  hgvsp: ENST00000533626.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000432489
  ensembl transcript: ENST00000531329
  gene symbol: EIF3F
  hgvsc: ENST00000531329.1:c.105G>A
  hgvsp: ENST00000531329.1:c.105G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3275
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12398
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1646
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1954
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35684
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2156
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala35Ala
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-8009006-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8009006
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8009006
    reference: chr 11
allele count: 2
allele frequency: 1.806619453678277e-5
allele num: 110704
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175390
  ensembl transcript: ENST00000528653
  gene symbol: EIF3F
  hgvsc: ENST00000528653.1:n.104C>T
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000431800
  ensembl transcript: ENST00000533626
  gene symbol: EIF3F
  hgvsc: ENST00000533626.1:c.107C>T
  hgvsp: ENSP00000431800.1:p.Ala36Val
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000396929
  ensembl transcript: ENST00000449102
  gene symbol: EIF3F
  hgvsc: ENST00000449102.2:c.-270C>T
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000442283
  ensembl transcript: ENST00000537635
  gene symbol: EIF3F
  hgvsc: ENST00000537635.1:c.152C>T
  hgvsp: ENSP00000442283.1:p.Ala51Val
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000432489
  ensembl transcript: ENST00000531329
  gene symbol: EIF3F
  hgvsc: ENST00000531329.1:c.107C>T
  hgvsp: ENSP00000432489.1:p.Ala36Val
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000310040
  ensembl transcript: ENST00000309828
  gene symbol: EIF3F
  hgvsc: ENST00000309828.4:c.107C>T
  hgvsp: ENSP00000310040.4:p.Ala36Val
  variant of: http://identifiers.org/hgnc/3275
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12457
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2823
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35114
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2146
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1631
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8015
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala36Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-71929599-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929599
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929599
    reference: chr 11
allele count: 4
allele frequency: 6.03172688340672e-5
allele num: 66316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.28-18C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.22-6C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.-24-6C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.28-6C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.-24-6C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.22-18C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.115-6C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.-30C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1630C>T
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16647
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8473
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3260
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 979
  bin: 7.5e0
  variant carriers: 0
hgvs: c.-24-6C>T
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

11-71929601-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929601
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929601
    reference: chr 11
allele count: 1
allele frequency: 1.470242295930369e-5
allele num: 68016
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.115-4C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.-24-4C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.22-16C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1632C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.28-16C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.22-4C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.-24-4C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.28-4C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.-28C>G
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25496
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17486
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18195
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3254
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 1.75e1
  variant carriers: 0
hgvs: c.-24-4C>G
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

11-71929602-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929602
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929602
    reference: chr 11
allele count: 1
allele frequency: 1.44108830989163e-5
allele num: 69392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.28-15T>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.115-3T>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1633T>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.-24-3T>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.28-3T>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.-24-3T>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.22-3T>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.-27T>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.22-15T>A
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18227
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25044
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8026
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3057
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3153
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1394
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 4.25e1
  variant carriers: 0
hgvs: c.-24-3T>A
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

11-71929608-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929608
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929608
    reference: chr 11
allele count: 554
allele frequency: 7.315269635028786e-3
allele num: 75732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.25C>T
  hgvsp: ENSP00000438568.1:p.Arg9Cys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.118C>T
  hgvsp: ENSP00000443307.1:p.Arg40Cys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.28-9C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.22-9C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.31C>T
  hgvsp: ENSP00000405638.2:p.Arg11Cys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.-21C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.-21C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1639C>T
  variant of: http://identifiers.org/hgnc/3793
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 21707
  bin: 2.25e1
  variant carriers: 110
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21958
  bin: 7.5e0
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 1.75e1
  variant carriers: 158
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7072
  bin: 1.25e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 3.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 3.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4748
  bin: 2.75e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2576
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg40Cys
num of homozygotes: 3
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

11-71929609-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929609
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929609
    reference: chr 11
allele count: 6
allele frequency: 7.757149506128149e-5
allele num: 77348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.119G>A
  hgvsp: ENSP00000443307.1:p.Arg40His
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.26G>A
  hgvsp: ENSP00000438568.1:p.Arg9His
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.22-8G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.-20G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.28-8G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.-20G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1640G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.32G>A
  hgvsp: ENSP00000405638.2:p.Arg11His
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.-20G>A
  variant of: http://identifiers.org/hgnc/3793
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6809
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22588
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2647
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23721
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2509
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg40His
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

11-71929609-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929609
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929609
    reference: chr 11
allele count: 4
allele frequency: 5.171433004085432e-5
allele num: 77348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1640G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.119G>T
  hgvsp: ENSP00000443307.1:p.Arg40Leu
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.22-8G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.26G>T
  hgvsp: ENSP00000438568.1:p.Arg9Leu
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.28-8G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.-20G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.32G>T
  hgvsp: ENSP00000405638.2:p.Arg11Leu
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.-20G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.-20G>T
  variant of: http://identifiers.org/hgnc/3793
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22588
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21232
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6809
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2509
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21864
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg40Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

11-71929620-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929620
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929620
    reference: chr 11
allele count: 2
allele frequency: 2.2237046920169e-5
allele num: 89940
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.37C>T
  hgvsp: ENSP00000438568.1:p.Gln13Ter
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.130C>T
  hgvsp: ENSP00000443307.1:p.Gln44Ter
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.25C>T
  hgvsp: ENSP00000441547.1:p.Gln9Ter
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.-9C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.-9C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1651C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.31C>T
  hgvsp: ENSP00000321957.7:p.Gln11Ter
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.43C>T
  hgvsp: ENSP00000405638.2:p.Gln15Ter
  variant of: http://identifiers.org/hgnc/3793
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2545
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31346
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gln11Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

11-71929626-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929626
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929626
    reference: chr 11
allele count: 2
allele frequency: 2.112780207475016e-5
allele num: 94662
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.-3G>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1657G>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.37G>C
  hgvsp: ENSP00000321957.7:p.Asp13His
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.49G>C
  hgvsp: ENSP00000405638.2:p.Asp17His
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.136G>C
  hgvsp: ENSP00000443307.1:p.Asp46His
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.31G>C
  hgvsp: ENSP00000441547.1:p.Asp11His
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.43G>C
  hgvsp: ENSP00000438568.1:p.Asp15His
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.-3G>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.-3G>C
  variant of: http://identifiers.org/hgnc/3793
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32008
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6426
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 890
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp13His
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD

11-8009008-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8009008
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8009008
    reference: chr 11
allele count: 6
allele frequency: 5.425445338638213e-5
allele num: 110590
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000310040
  ensembl transcript: ENST00000309828
  gene symbol: EIF3F
  hgvsc: ENST00000309828.4:c.109C>G
  hgvsp: ENSP00000310040.4:p.Pro37Ala
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000442283
  ensembl transcript: ENST00000537635
  gene symbol: EIF3F
  hgvsc: ENST00000537635.1:c.154C>G
  hgvsp: ENSP00000442283.1:p.Pro52Ala
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000431800
  ensembl transcript: ENST00000533626
  gene symbol: EIF3F
  hgvsc: ENST00000533626.1:c.109C>G
  hgvsp: ENSP00000431800.1:p.Pro37Ala
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175390
  ensembl transcript: ENST00000528653
  gene symbol: EIF3F
  hgvsc: ENST00000528653.1:n.106C>G
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000432489
  ensembl transcript: ENST00000531329
  gene symbol: EIF3F
  hgvsc: ENST00000531329.1:c.109C>G
  hgvsp: ENSP00000432489.1:p.Pro37Ala
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000396929
  ensembl transcript: ENST00000449102
  gene symbol: EIF3F
  hgvsc: ENST00000449102.2:c.-268C>G
  variant of: http://identifiers.org/hgnc/3275
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9387
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12529
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7974
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1617
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2126
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro37Ala
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: C
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

11-8009015-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 8009015
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 8009015
    reference: chr 11
allele count: 2580
allele frequency: 2.343153994260181e-2
allele num: 110108
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000431800
  ensembl transcript: ENST00000533626
  gene symbol: EIF3F
  hgvsc: ENST00000533626.1:c.116C>T
  hgvsp: ENSP00000431800.1:p.Pro39Leu
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000432489
  ensembl transcript: ENST00000531329
  gene symbol: EIF3F
  hgvsc: ENST00000531329.1:c.116C>T
  hgvsp: ENSP00000432489.1:p.Pro39Leu
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000442283
  ensembl transcript: ENST00000537635
  gene symbol: EIF3F
  hgvsc: ENST00000537635.1:c.161C>T
  hgvsp: ENSP00000442283.1:p.Pro54Leu
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000310040
  ensembl transcript: ENST00000309828
  gene symbol: EIF3F
  hgvsc: ENST00000309828.4:c.116C>T
  hgvsp: ENSP00000310040.4:p.Pro39Leu
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000175390
  ensembl protein: ENSP00000396929
  ensembl transcript: ENST00000449102
  gene symbol: EIF3F
  hgvsc: ENST00000449102.2:c.-261C>T
  variant of: http://identifiers.org/hgnc/3275
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175390
  ensembl transcript: ENST00000528653
  gene symbol: EIF3F
  hgvsc: ENST00000528653.1:n.113C>T
  variant of: http://identifiers.org/hgnc/3275
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 25413
  bin: 2.75e1
  variant carriers: 144
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 1.75e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 8984
  bin: 3.25e1
  variant carriers: 214
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2328
  bin: 1.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.75e1
  variant carriers: 124
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 7.5e0
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 202
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 294
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 5.25e1
  variant carriers: 273
genotype depth: GenotypeDepth
  all individuals: 12841
  bin: 2.25e1
  variant carriers: 130
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.25e1
  variant carriers: 150
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.75e1
  variant carriers: 260
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 288
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 4.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 34572
  bin: 6.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1715
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2020
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2979
  bin: 2.25e1
  variant carriers: 3
hgvs: p.Pro39Leu
num of homozygotes: 48
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

11-71929661-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929661
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929661
    reference: chr 11
allele count: 1
allele frequency: 9.500826571911757e-6
allele num: 105254
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.171T>C
  hgvsp: ENST00000541003.1:c.171T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.33T>C
  hgvsp: ENST00000538353.1:c.33T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.78T>C
  hgvsp: ENST00000536778.1:c.78T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.66T>C
  hgvsp: ENST00000539412.1:c.66T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.33T>C
  hgvsp: ENST00000298223.6:c.33T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.84T>C
  hgvsp: ENST00000449475.2:c.84T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1692T>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.33T>C
  hgvsp: ENST00000535625.1:c.33T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.72T>C
  hgvsp: ENST00000321324.7:c.72T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7993
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8613
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1015
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu11Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

11-71929665-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929665
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929665
    reference: chr 11
allele count: 2
allele frequency: 1.893473197886884e-5
allele num: 105626
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.37G>A
  hgvsp: ENSP00000298223.6:p.Val13Ile
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.37G>A
  hgvsp: ENSP00000444794.1:p.Val13Ile
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.37G>A
  hgvsp: ENSP00000440337.1:p.Val13Ile
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.82G>A
  hgvsp: ENSP00000438568.1:p.Val28Ile
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1696G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.70G>A
  hgvsp: ENSP00000441547.1:p.Val24Ile
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.88G>A
  hgvsp: ENSP00000405638.2:p.Val30Ile
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.175G>A
  hgvsp: ENSP00000443307.1:p.Val59Ile
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.76G>A
  hgvsp: ENSP00000321957.7:p.Val26Ile
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2943
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7771
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34248
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1214
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 861
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 590
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Val13Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

11-71929666-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929666
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929666
    reference: chr 11
allele count: 8
allele frequency: 7.568876778686043e-5
allele num: 105696
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.83T>A
  hgvsp: ENSP00000438568.1:p.Val28Asp
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.38T>A
  hgvsp: ENSP00000444794.1:p.Val13Asp
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.38T>A
  hgvsp: ENSP00000298223.6:p.Val13Asp
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.71T>A
  hgvsp: ENSP00000441547.1:p.Val24Asp
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.89T>A
  hgvsp: ENSP00000405638.2:p.Val30Asp
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.77T>A
  hgvsp: ENSP00000321957.7:p.Val26Asp
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.176T>A
  hgvsp: ENSP00000443307.1:p.Val59Asp
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1697T>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.38T>A
  hgvsp: ENSP00000440337.1:p.Val13Asp
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3720
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7745
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8816
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34120
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3036
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1362
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 887
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 9.75e1
  variant carriers: 8
hgvs: p.Val13Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

11-71929674-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929674
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929674
    reference: chr 11
allele count: 1
allele frequency: 9.461095973357553e-6
allele num: 105696
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.91G>A
  hgvsp: ENSP00000438568.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.97G>A
  hgvsp: ENSP00000405638.2:p.Ala33Thr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.85G>A
  hgvsp: ENSP00000321957.7:p.Ala29Thr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.46G>A
  hgvsp: ENSP00000440337.1:p.Ala16Thr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.46G>A
  hgvsp: ENSP00000444794.1:p.Ala16Thr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.46G>A
  hgvsp: ENSP00000298223.6:p.Ala16Thr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.184G>A
  hgvsp: ENSP00000443307.1:p.Ala62Thr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1705G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.79G>A
  hgvsp: ENSP00000441547.1:p.Ala27Thr
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4037
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32019
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1466
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1711
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34656
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala16Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

11-71929684-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929684
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929684
    reference: chr 11
allele count: 11
allele frequency: 1.043187982474442e-4
allele num: 105446
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.194G>A
  hgvsp: ENSP00000443307.1:p.Cys65Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.56G>A
  hgvsp: ENSP00000444794.1:p.Cys19Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.101G>A
  hgvsp: ENSP00000438568.1:p.Cys34Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1715G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.95G>A
  hgvsp: ENSP00000321957.7:p.Cys32Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.56G>A
  hgvsp: ENSP00000440337.1:p.Cys19Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.89G>A
  hgvsp: ENSP00000441547.1:p.Cys30Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.56G>A
  hgvsp: ENSP00000298223.6:p.Cys19Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.107G>A
  hgvsp: ENSP00000405638.2:p.Cys36Tyr
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5167
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30186
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7757
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10599
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1635
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Cys19Tyr
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum

11-71929687-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929687
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929687
    reference: chr 11
allele count: 1
allele frequency: 9.488026111047858e-6
allele num: 105396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.92G>A
  hgvsp: ENSP00000441547.1:p.Ser31Asn
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.98G>A
  hgvsp: ENSP00000321957.7:p.Ser33Asn
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.110G>A
  hgvsp: ENSP00000405638.2:p.Ser37Asn
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.59G>A
  hgvsp: ENSP00000440337.1:p.Ser20Asn
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.59G>A
  hgvsp: ENSP00000298223.6:p.Ser20Asn
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1718G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.197G>A
  hgvsp: ENSP00000443307.1:p.Ser66Asn
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.59G>A
  hgvsp: ENSP00000444794.1:p.Ser20Asn
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.104G>A
  hgvsp: ENSP00000438568.1:p.Ser35Asn
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7806
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5402
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5242
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2831
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1605
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1687
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser20Asn
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

11-71929688-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929688
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929688
    reference: chr 11
allele count: 1
allele frequency: 9.492168960607498e-6
allele num: 105350
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.60T>G
  hgvsp: ENSP00000298223.6:p.Ser20Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.99T>G
  hgvsp: ENSP00000321957.7:p.Ser33Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1719T>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.198T>G
  hgvsp: ENSP00000443307.1:p.Ser66Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.111T>G
  hgvsp: ENSP00000405638.2:p.Ser37Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.60T>G
  hgvsp: ENSP00000444794.1:p.Ser20Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.93T>G
  hgvsp: ENSP00000441547.1:p.Ser31Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.105T>G
  hgvsp: ENSP00000438568.1:p.Ser35Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.60T>G
  hgvsp: ENSP00000440337.1:p.Ser20Arg
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7885
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5377
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ser20Arg
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

11-71929695-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929695
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929695
    reference: chr 11
allele count: 2
allele frequency: 1.911388050001911e-5
allele num: 104636
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.67G>A
  hgvsp: ENSP00000298223.6:p.Asp23Asn
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.118G>A
  hgvsp: ENSP00000405638.2:p.Asp40Asn
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.106G>A
  hgvsp: ENSP00000321957.7:p.Asp36Asn
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.205G>A
  hgvsp: ENSP00000443307.1:p.Asp69Asn
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.112G>A
  hgvsp: ENSP00000438568.1:p.Asp38Asn
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.67G>A
  hgvsp: ENSP00000444794.1:p.Asp23Asn
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.67G>A
  hgvsp: ENSP00000440337.1:p.Asp23Asn
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.100G>A
  hgvsp: ENSP00000441547.1:p.Asp34Asn
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1726G>A
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5952
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28338
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8919
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30879
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp23Asn
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-71929703-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929703
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929703
    reference: chr 11
allele count: 1
allele frequency: 9.597297401051864e-6
allele num: 104196
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.126T>G
  hgvsp: ENST00000449475.2:c.126T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.108T>G
  hgvsp: ENST00000539412.1:c.108T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.75T>G
  hgvsp: ENST00000298223.6:c.75T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.120T>G
  hgvsp: ENST00000536778.1:c.120T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.75T>G
  hgvsp: ENST00000535625.1:c.75T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.114T>G
  hgvsp: ENST00000321324.7:c.114T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1734T>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.213T>G
  hgvsp: ENST00000541003.1:c.213T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.75T>G
  hgvsp: ENST00000538353.1:c.75T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5825
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8624
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6469
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1854
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1902
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr25Thr
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: T
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-71929705-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929705
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929705
    reference: chr 11
allele count: 1
allele frequency: 9.617604062475956e-6
allele num: 103976
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.77A>G
  hgvsp: ENSP00000444794.1:p.Asp26Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.116A>G
  hgvsp: ENSP00000321957.7:p.Asp39Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.77A>G
  hgvsp: ENSP00000440337.1:p.Asp26Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.77A>G
  hgvsp: ENSP00000298223.6:p.Asp26Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.215A>G
  hgvsp: ENSP00000443307.1:p.Asp72Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.128A>G
  hgvsp: ENSP00000405638.2:p.Asp43Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.122A>G
  hgvsp: ENSP00000438568.1:p.Asp41Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.110A>G
  hgvsp: ENSP00000441547.1:p.Asp37Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1736A>G
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5894
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8510
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6631
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1882
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12212
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp26Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-71929706-TCTC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929706
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929703
    reference: chr 11
allele count: 1
allele frequency: 9.612796554773715e-6
allele num: 104028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.133_135delCTC
  hgvsp: ENSP00000405638.2:p.Leu45del
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.82_84delCTC
  hgvsp: ENSP00000440337.1:p.Leu28del
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1741_27+1743delCTC
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.121_123delCTC
  hgvsp: ENSP00000321957.7:p.Leu41del
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.82_84delCTC
  hgvsp: ENSP00000298223.6:p.Leu28del
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.127_129delCTC
  hgvsp: ENSP00000438568.1:p.Leu43del
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.82_84delCTC
  hgvsp: ENSP00000444794.1:p.Leu28del
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.220_222delCTC
  hgvsp: ENSP00000443307.1:p.Leu74del
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.115_117delCTC
  hgvsp: ENSP00000441547.1:p.Leu39del
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8506
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1808
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2216
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu28del
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: TCTC
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ

11-71929710-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929710
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929710
    reference: chr 11
allele count: 2
allele frequency: 1.928342782212966e-5
allele num: 103716
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.115C>T
  hgvsp: ENSP00000441547.1:p.Leu39Phe
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.82C>T
  hgvsp: ENSP00000444794.1:p.Leu28Phe
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.121C>T
  hgvsp: ENSP00000321957.7:p.Leu41Phe
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.82C>T
  hgvsp: ENSP00000440337.1:p.Leu28Phe
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.133C>T
  hgvsp: ENSP00000405638.2:p.Leu45Phe
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1741C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.127C>T
  hgvsp: ENSP00000438568.1:p.Leu43Phe
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.82C>T
  hgvsp: ENSP00000298223.6:p.Leu28Phe
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.220C>T
  hgvsp: ENSP00000443307.1:p.Leu74Phe
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8596
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8601
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6793
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2611
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31421
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1910
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu28Phe
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-71929712-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929712
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929712
    reference: chr 11
allele count: 18
allele frequency: 1.740004640012373e-4
allele num: 103448
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.222C>T
  hgvsp: ENST00000541003.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.123C>T
  hgvsp: ENST00000321324.7:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.135C>T
  hgvsp: ENST00000449475.2:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.129C>T
  hgvsp: ENST00000536778.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1743C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.84C>T
  hgvsp: ENST00000298223.6:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.117C>T
  hgvsp: ENST00000539412.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.84C>T
  hgvsp: ENST00000538353.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.84C>T
  hgvsp: ENST00000535625.1:c.84C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28071
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6907
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5216
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8587
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2184
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1551
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu28Leu
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD

11-71929720-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929720
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929720
    reference: chr 11
allele count: 2
allele frequency: 1.950534446438324e-5
allele num: 102536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.125G>A
  hgvsp: ENSP00000441547.1:p.Cys42Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.92G>A
  hgvsp: ENSP00000440337.1:p.Cys31Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.137G>A
  hgvsp: ENSP00000438568.1:p.Cys46Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1751G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.143G>A
  hgvsp: ENSP00000405638.2:p.Cys48Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.92G>A
  hgvsp: ENSP00000298223.6:p.Cys31Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.230G>A
  hgvsp: ENSP00000443307.1:p.Cys77Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.92G>A
  hgvsp: ENSP00000444794.1:p.Cys31Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.131G>A
  hgvsp: ENSP00000321957.7:p.Cys44Tyr
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4950
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2560
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Cys31Tyr
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-71929720-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929720
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929720
    reference: chr 11
allele count: 1
allele frequency: 9.75267223219162e-6
allele num: 102536
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.131G>C
  hgvsp: ENSP00000321957.7:p.Cys44Ser
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.92G>C
  hgvsp: ENSP00000440337.1:p.Cys31Ser
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.125G>C
  hgvsp: ENSP00000441547.1:p.Cys42Ser
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.137G>C
  hgvsp: ENSP00000438568.1:p.Cys46Ser
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.92G>C
  hgvsp: ENSP00000298223.6:p.Cys31Ser
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.143G>C
  hgvsp: ENSP00000405638.2:p.Cys48Ser
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.230G>C
  hgvsp: ENSP00000443307.1:p.Cys77Ser
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.92G>C
  hgvsp: ENSP00000444794.1:p.Cys31Ser
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1751G>C
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4950
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1452
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2207
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1458
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Cys31Ser
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP

11-71929750-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929750
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929750
    reference: chr 11
allele count: 1
allele frequency: 1.023017902813299e-5
allele num: 97750
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.122C>G
  hgvsp: ENSP00000298223.6:p.Pro41Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.167C>G
  hgvsp: ENSP00000438568.1:p.Pro56Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.260C>G
  hgvsp: ENSP00000443307.1:p.Pro87Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.122C>G
  hgvsp: ENSP00000444794.1:p.Pro41Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.161C>G
  hgvsp: ENSP00000321957.7:p.Pro54Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.122C>G
  hgvsp: ENSP00000440337.1:p.Pro41Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1781C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.173C>G
  hgvsp: ENSP00000405638.2:p.Pro58Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.155C>G
  hgvsp: ENSP00000441547.1:p.Pro52Arg
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7688
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9861
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro41Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

11-71929752-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929752
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929752
    reference: chr 11
allele count: 1
allele frequency: 1.02819305352773e-5
allele num: 97258
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.169G>C
  hgvsp: ENSP00000438568.1:p.Gly57Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.157G>C
  hgvsp: ENSP00000441547.1:p.Gly53Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.124G>C
  hgvsp: ENSP00000298223.6:p.Gly42Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.262G>C
  hgvsp: ENSP00000443307.1:p.Gly88Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.124G>C
  hgvsp: ENSP00000440337.1:p.Gly42Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.124G>C
  hgvsp: ENSP00000444794.1:p.Gly42Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1783G>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.163G>C
  hgvsp: ENSP00000321957.7:p.Gly55Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.175G>C
  hgvsp: ENSP00000405638.2:p.Gly59Arg
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11693
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3035
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2221
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2290
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly42Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

11-71929770-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929770
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929770
    reference: chr 11
allele count: 1
allele frequency: 1.09051254089422e-5
allele num: 91700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.142C>T
  hgvsp: ENSP00000440337.1:p.His48Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.142C>T
  hgvsp: ENSP00000298223.6:p.His48Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1801C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.280C>T
  hgvsp: ENSP00000443307.1:p.His94Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.193C>T
  hgvsp: ENSP00000405638.2:p.His65Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.187C>T
  hgvsp: ENSP00000438568.1:p.His63Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.175C>T
  hgvsp: ENSP00000441547.1:p.His59Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.142C>T
  hgvsp: ENSP00000444794.1:p.His48Tyr
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.181C>T
  hgvsp: ENSP00000321957.7:p.His61Tyr
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13715
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2865
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His48Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

11-71929782-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929782
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929782
    reference: chr 11
allele count: 11
allele frequency: 1.273236567354214e-4
allele num: 86394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.195+4C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1813C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.150+4C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.189+4C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.288+4C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.183+4C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.201+4C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.150+4C>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.150+4C>T
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5683
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13941
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16048
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3221
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1532
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17771
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 7.5e0
  variant carriers: 0
hgvs: c.150+4C>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

11-71929783-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929783
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929783
    reference: chr 11
allele count: 14
allele frequency: 1.625751910258494e-4
allele num: 86114
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.288+5G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.195+5G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.201+5G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.150+5G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.150+5G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.150+5G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.189+5G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1814G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.183+5G>A
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17998
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13745
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 8.25e1
  variant carriers: 0
hgvs: c.150+5G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP

11-71929783-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929783
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929783
    reference: chr 11
allele count: 1
allele frequency: 1.161251364470353e-5
allele num: 86114
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.288+5G>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.195+5G>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.189+5G>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1814G>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.150+5G>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.150+5G>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.183+5G>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.201+5G>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.150+5G>C
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17998
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3786
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
hgvs: c.150+5G>C
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-71929784-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929784
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929784
    reference: chr 11
allele count: 2
allele frequency: 2.343621833180998e-5
allele num: 85338
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.150+6G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.150+6G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1815G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.288+6G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.189+6G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.183+6G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.150+6G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.201+6G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.195+6G>T
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3254
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18528
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13003
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 922
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 971
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 6.75e1
  variant carriers: 0
hgvs: c.150+6G>T
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/11-71929785-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929785
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929785
    reference: chr 11
allele count: 1
allele frequency: 1.173819137947225e-5
allele num: 85192
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.150+7C>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1816C>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.189+7C>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.195+7C>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.201+7C>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.183+7C>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.288+7C>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.150+7C>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.150+7C>A
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13018
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16495
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3160
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26672
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1381
  bin: 7.5e0
  variant carriers: 0
hgvs: c.150+7C>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

11-71929787-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929787
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929787
    reference: chr 11
allele count: 52
allele frequency: 6.125141349415756e-4
allele num: 84896
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1818G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.288+9G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.183+9G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.195+9G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.150+9G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.189+9G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.201+9G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.150+9G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.150+9G>A
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12884
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18704
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 16619
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1602
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26997
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

11-71929804-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929804
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929804
    reference: chr 11
allele count: 1
allele frequency: 1.290822253775655e-5
allele num: 77470
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1835A>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.150+26A>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.183+26A>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.288+26A>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.195+26A>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.150+26A>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.201+26A>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.189+26A>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.150+26A>G
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21259
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5296
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2393
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

11-71929807-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929807
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929806
    reference: chr 11
allele count: 20
allele frequency: 2.646833064238639e-4
allele num: 75562
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.150+34delG
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.183+34delG
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.201+34delG
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1843delG
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.150+34delG
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.189+34delG
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.195+34delG
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.150+34delG
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.288+34delG
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18435
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20984
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4895
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3380
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7724
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2630
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1947
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 7.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: AG
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

11-71929811-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71929811
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71929811
    reference: chr 11
allele count: 1
allele frequency: 1.367240907847963e-5
allele num: 73140
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.27+1842G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.150+33G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.183+33G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.189+33G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.150+33G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.195+33G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.201+33G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.150+33G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.288+33G>A
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20316
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4411
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19071
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24549
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4837
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum

11-71931871-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931871
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931871
    reference: chr 11
allele count: 1
allele frequency: 8.588556607176597e-6
allele num: 116434
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.202-43G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.28-43G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.289-43G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.151-43G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.184-43G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.151-43G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.151-43G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.196-43G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.190-43G>A
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11686
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8953
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9513
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26821
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 875
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2548
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2172
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3705
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

11-71931873-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931873
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931873
    reference: chr 11
allele count: 5
allele frequency: 4.294942275975811e-5
allele num: 116416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.196-41G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.184-41G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.151-41G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.190-41G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.151-41G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.151-41G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.202-41G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.28-41G>T
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.289-41G>T
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11983
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5602
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8577
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21770
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7611
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1020
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4203
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2119
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5778
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-71931875-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931875
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931875
    reference: chr 11
allele count: 3
allele frequency: 2.572678157962439e-5
allele num: 116610
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.151-39G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.202-39G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.28-39G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.184-39G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.196-39G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.151-39G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.151-39G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.190-39G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.289-39G>A
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23021
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6456
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2084
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3051
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3840
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum

11-71931877-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931877
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931877
    reference: chr 11
allele count: 1
allele frequency: 8.556808652644909e-6
allele num: 116866
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.151-37A>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.28-37A>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.151-37A>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.151-37A>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.190-37A>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.202-37A>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.289-37A>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.184-37A>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.196-37A>G
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5058
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 692
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1725
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6521
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1498
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

11-71931880-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931880
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931880
    reference: chr 11
allele count: 2
allele frequency: 1.709781660881905e-5
allele num: 116974
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.28-34G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.151-34G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.184-34G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.202-34G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.151-34G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.289-34G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.190-34G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.196-34G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.151-34G>A
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6144
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14165
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3468
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25623
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1698
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2568
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6631
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/11-71931887-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931887
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931887
    reference: chr 11
allele count: 1
allele frequency: 8.487379267029927e-6
allele num: 117822
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.190-27A>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.151-27A>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.202-27A>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.184-27A>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.289-27A>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.151-27A>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.28-27A>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.151-27A>C
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.196-27A>C
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28581
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3915
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15356
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1901
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: A
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-71931888-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931888
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931888
    reference: chr 11
allele count: 1
allele frequency: 8.480901010923401e-6
allele num: 117912
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.184-26C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.289-26C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.190-26C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.202-26C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.196-26C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.151-26C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.28-26C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.151-26C>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.151-26C>G
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1074
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1975
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP

11-71931896-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931896
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931896
    reference: chr 11
allele count: 16
allele frequency: 1.34661998384056e-4
allele num: 118816
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.184-18T>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.202-18T>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.289-18T>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.151-18T>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.190-18T>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.28-18T>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.196-18T>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.151-18T>G
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.151-18T>G
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16285
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6818
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1103
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

11-71931897-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931897
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931897
    reference: chr 11
allele count: 1
allele frequency: 8.409155888931868e-6
allele num: 118918
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.184-17G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.28-17G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.289-17G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.151-17G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.151-17G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.202-17G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.151-17G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.196-17G>A
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.190-17G>A
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30529
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6842
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41494
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1108
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2009
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

11-71931922-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931922
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931923
    reference: chr 11
allele count: 1
allele frequency: 8.324038157390913e-6
allele num: 120134
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.160dupT
  hgvsp: ENSP00000444794.1:p.Trp54LeufsTer26
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.193dupT
  hgvsp: ENSP00000441547.1:p.Trp65LeufsTer26
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.211dupT
  hgvsp: ENSP00000405638.2:p.Trp71LeufsTer26
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.199dupT
  hgvsp: ENSP00000321957.7:p.Trp67LeufsTer26
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.37dupT
  hgvsp: ENSP00000414094.2:p.Trp13LeufsTer26
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.160dupT
  hgvsp: ENSP00000298223.6:p.Trp54LeufsTer26
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.298dupT
  hgvsp: ENSP00000443307.1:p.Trp100LeufsTer26
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.205dupT
  hgvsp: ENSP00000438568.1:p.Trp69LeufsTer26
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.160dupT
  hgvsp: ENSP00000440337.1:p.Trp54LeufsTer26
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2162
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Trp54LeufsTer26
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

11-71931924-GGAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931924
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931921
    reference: chr 11
allele count: 10
allele frequency: 8.320852055250458e-5
allele num: 120180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.45_47delGAA
  hgvsp: ENSP00000414094.2:p.Lys15del
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.219_221delGAA
  hgvsp: ENSP00000405638.2:p.Lys73del
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.168_170delGAA
  hgvsp: ENSP00000440337.1:p.Lys56del
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.213_215delGAA
  hgvsp: ENSP00000438568.1:p.Lys71del
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.168_170delGAA
  hgvsp: ENSP00000298223.6:p.Lys56del
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.306_308delGAA
  hgvsp: ENSP00000443307.1:p.Lys102del
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.168_170delGAA
  hgvsp: ENSP00000444794.1:p.Lys56del
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.201_203delGAA
  hgvsp: ENSP00000441547.1:p.Lys67del
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.207_209delGAA
  hgvsp: ENSP00000321957.7:p.Lys69del
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7242
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2245
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42944
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys56del
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: GGAA
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP

11-71931925-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931925
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931925
    reference: chr 11
allele count: 1
allele frequency: 8.320575118152166e-6
allele num: 120184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.195G>A
  hgvsp: ENSP00000441547.1:p.Trp65Ter
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.162G>A
  hgvsp: ENSP00000444794.1:p.Trp54Ter
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.162G>A
  hgvsp: ENSP00000440337.1:p.Trp54Ter
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.300G>A
  hgvsp: ENSP00000443307.1:p.Trp100Ter
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.162G>A
  hgvsp: ENSP00000298223.6:p.Trp54Ter
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.201G>A
  hgvsp: ENSP00000321957.7:p.Trp67Ter
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.213G>A
  hgvsp: ENSP00000405638.2:p.Trp71Ter
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.39G>A
  hgvsp: ENSP00000414094.2:p.Trp13Ter
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.207G>A
  hgvsp: ENSP00000438568.1:p.Trp69Ter
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Trp54Ter
num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

11-71931938-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931938
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931938
    reference: chr 11
allele count: 1
allele frequency: 8.31255195344971e-6
allele num: 120300
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.226T>C
  hgvsp: ENSP00000405638.2:p.Cys76Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.52T>C
  hgvsp: ENSP00000414094.2:p.Cys18Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.175T>C
  hgvsp: ENSP00000298223.6:p.Cys59Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.313T>C
  hgvsp: ENSP00000443307.1:p.Cys105Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.175T>C
  hgvsp: ENSP00000440337.1:p.Cys59Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.220T>C
  hgvsp: ENSP00000438568.1:p.Cys74Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.175T>C
  hgvsp: ENSP00000444794.1:p.Cys59Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.214T>C
  hgvsp: ENSP00000321957.7:p.Cys72Arg
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.208T>C
  hgvsp: ENSP00000441547.1:p.Cys70Arg
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7315
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29648
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7915
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys59Arg
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-71931945-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931945
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931945
    reference: chr 11
allele count: 9
allele frequency: 7.485403463246669e-5
allele num: 120234
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.227C>A
  hgvsp: ENSP00000438568.1:p.Thr76Lys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.182C>A
  hgvsp: ENSP00000440337.1:p.Thr61Lys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.215C>A
  hgvsp: ENSP00000441547.1:p.Thr72Lys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.221C>A
  hgvsp: ENSP00000321957.7:p.Thr74Lys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.233C>A
  hgvsp: ENSP00000405638.2:p.Thr78Lys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.59C>A
  hgvsp: ENSP00000414094.2:p.Thr20Lys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.182C>A
  hgvsp: ENSP00000298223.6:p.Thr61Lys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.182C>A
  hgvsp: ENSP00000444794.1:p.Thr61Lys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.320C>A
  hgvsp: ENSP00000443307.1:p.Thr107Lys
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18869
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr61Lys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-71931945-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931945
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931945
    reference: chr 11
allele count: 1
allele frequency: 8.317114959162966e-6
allele num: 120234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.320C>T
  hgvsp: ENSP00000443307.1:p.Thr107Ile
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.182C>T
  hgvsp: ENSP00000298223.6:p.Thr61Ile
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.233C>T
  hgvsp: ENSP00000405638.2:p.Thr78Ile
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.227C>T
  hgvsp: ENSP00000438568.1:p.Thr76Ile
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.182C>T
  hgvsp: ENSP00000440337.1:p.Thr61Ile
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.59C>T
  hgvsp: ENSP00000414094.2:p.Thr20Ile
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.182C>T
  hgvsp: ENSP00000444794.1:p.Thr61Ile
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.221C>T
  hgvsp: ENSP00000321957.7:p.Thr74Ile
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.215C>T
  hgvsp: ENSP00000441547.1:p.Thr72Ile
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7539
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7487
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr61Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

11-71931946-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931946
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931946
    reference: chr 11
allele count: 53
allele frequency: 4.416666666666667e-4
allele num: 120000
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.216A>G
  hgvsp: ENST00000539412.1:c.216A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.222A>G
  hgvsp: ENST00000321324.7:c.222A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.60A>G
  hgvsp: ENST00000454954.2:c.60A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.321A>G
  hgvsp: ENST00000541003.1:c.321A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.234A>G
  hgvsp: ENST00000449475.2:c.234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.183A>G
  hgvsp: ENST00000298223.6:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.228A>G
  hgvsp: ENST00000536778.1:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.183A>G
  hgvsp: ENST00000538353.1:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.183A>G
  hgvsp: ENST00000535625.1:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28197
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7532
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18887
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1231
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 2.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 7449
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.75e1
  variant carriers: 1
hgvs: p.Thr61Thr
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

11-71931950-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931950
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931950
    reference: chr 11
allele count: 1
allele frequency: 8.313795912937929e-6
allele num: 120282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.226A>G
  hgvsp: ENSP00000321957.7:p.Ser76Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.238A>G
  hgvsp: ENSP00000405638.2:p.Ser80Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.232A>G
  hgvsp: ENSP00000438568.1:p.Ser78Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.187A>G
  hgvsp: ENSP00000444794.1:p.Ser63Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.187A>G
  hgvsp: ENSP00000440337.1:p.Ser63Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.64A>G
  hgvsp: ENSP00000414094.2:p.Ser22Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.187A>G
  hgvsp: ENSP00000298223.6:p.Ser63Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.325A>G
  hgvsp: ENSP00000443307.1:p.Ser109Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.220A>G
  hgvsp: ENSP00000441547.1:p.Ser74Gly
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 28205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19112
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2120
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 560
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser63Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

11-71931955-CAGCCAGG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931955
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931948
    reference: chr 11
allele count: 1
allele frequency: 8.311861025683651e-6
allele num: 120310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.73_79delCAGGAGC
  hgvsp: ENSP00000414094.2:p.Gln25CysfsTer47
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.235_241delCAGGAGC
  hgvsp: ENSP00000321957.7:p.Gln79CysfsTer47
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.196_202delCAGGAGC
  hgvsp: ENSP00000298223.6:p.Gln66CysfsTer47
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.196_202delCAGGAGC
  hgvsp: ENSP00000440337.1:p.Gln66CysfsTer47
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.196_202delCAGGAGC
  hgvsp: ENSP00000444794.1:p.Gln66CysfsTer47
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.241_247delCAGGAGC
  hgvsp: ENSP00000438568.1:p.Gln81CysfsTer47
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.334_340delCAGGAGC
  hgvsp: ENSP00000443307.1:p.Gln112CysfsTer?
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.247_253delCAGGAGC
  hgvsp: ENSP00000405638.2:p.Gln83CysfsTer47
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.229_235delCAGGAGC
  hgvsp: ENSP00000441547.1:p.Gln77CysfsTer47
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19366
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1030
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2142
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gln66CysfsTer47
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: CAGCCAGG
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

11-71931962-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931962
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931962
    reference: chr 11
allele count: 1
allele frequency: 8.307993951780402e-6
allele num: 120366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.199G>A
  hgvsp: ENSP00000440337.1:p.Glu67Lys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.199G>A
  hgvsp: ENSP00000298223.6:p.Glu67Lys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.250G>A
  hgvsp: ENSP00000405638.2:p.Glu84Lys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.244G>A
  hgvsp: ENSP00000438568.1:p.Glu82Lys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.337G>A
  hgvsp: ENSP00000443307.1:p.Glu113Lys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.232G>A
  hgvsp: ENSP00000441547.1:p.Glu78Lys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.238G>A
  hgvsp: ENSP00000321957.7:p.Glu80Lys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.76G>A
  hgvsp: ENSP00000414094.2:p.Glu26Lys
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.199G>A
  hgvsp: ENSP00000444794.1:p.Glu67Lys
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19388
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7515
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu67Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

11-71931963-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931963
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931963
    reference: chr 11
allele count: 3
allele frequency: 2.492646692257839e-5
allele num: 120354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.200A>G
  hgvsp: ENSP00000444794.1:p.Glu67Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.251A>G
  hgvsp: ENSP00000405638.2:p.Glu84Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.245A>G
  hgvsp: ENSP00000438568.1:p.Glu82Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.77A>G
  hgvsp: ENSP00000414094.2:p.Glu26Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.200A>G
  hgvsp: ENSP00000440337.1:p.Glu67Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.239A>G
  hgvsp: ENSP00000321957.7:p.Glu80Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.200A>G
  hgvsp: ENSP00000298223.6:p.Glu67Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.233A>G
  hgvsp: ENSP00000441547.1:p.Glu78Gly
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.338A>G
  hgvsp: ENSP00000443307.1:p.Glu113Gly
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7495
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1557
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27616
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1033
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu67Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/11-71931977-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931977
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931977
    reference: chr 11
allele count: 793
allele frequency: 7.665242523247047e-3
allele num: 103454
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.265A>C
  hgvsp: ENSP00000405638.2:p.Thr89Pro
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.214A>C
  hgvsp: ENSP00000440337.1:p.Thr72Pro
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.214A>C
  hgvsp: ENSP00000444794.1:p.Thr72Pro
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.352A>C
  hgvsp: ENSP00000443307.1:p.Thr118Pro
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.259A>C
  hgvsp: ENSP00000438568.1:p.Thr87Pro
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.247A>C
  hgvsp: ENSP00000441547.1:p.Thr83Pro
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.253A>C
  hgvsp: ENSP00000321957.7:p.Thr85Pro
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.214A>C
  hgvsp: ENSP00000298223.6:p.Thr72Pro
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.91A>C
  hgvsp: ENSP00000414094.2:p.Thr31Pro
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 19652
  bin: 2.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 17477
  bin: 2.75e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 5.25e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 4.25e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 3.75e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.25e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 3137
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 5.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 9626
  bin: 3.25e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 57
genotype quality: GenotypeQuality
  all individuals: 2353
  bin: 4.25e1
  variant carriers: 48
genotype quality: GenotypeQuality
  all individuals: 4816
  bin: 2.5e0
  variant carriers: 25
genotype quality: GenotypeQuality
  all individuals: 2190
  bin: 2.25e1
  variant carriers: 41
genotype quality: GenotypeQuality
  all individuals: 2325
  bin: 3.25e1
  variant carriers: 51
hgvs: p.Thr72Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

11-71931980-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 71931980
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 71931980
    reference: chr 11
allele count: 5
allele frequency: 4.181371155229223e-5
allele num: 119578
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000321957
  ensembl transcript: ENST00000321324
  gene symbol: FOLR2
  hgvsc: ENST00000321324.7:c.256T>C
  hgvsp: ENSP00000321957.7:p.Ser86Pro
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000405638
  ensembl transcript: ENST00000449475
  gene symbol: FOLR2
  hgvsc: ENST00000449475.2:c.268T>C
  hgvsp: ENSP00000405638.2:p.Ser90Pro
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000443307
  ensembl transcript: ENST00000541003
  gene symbol: FOLR2
  hgvsc: ENST00000541003.1:c.355T>C
  hgvsp: ENSP00000443307.1:p.Ser119Pro
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000444794
  ensembl transcript: ENST00000535625
  gene symbol: FOLR2
  hgvsc: ENST00000535625.1:c.217T>C
  hgvsp: ENSP00000444794.1:p.Ser73Pro
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000440337
  ensembl transcript: ENST00000538353
  gene symbol: FOLR2
  hgvsc: ENST00000538353.1:c.217T>C
  hgvsp: ENSP00000440337.1:p.Ser73Pro
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000414094
  ensembl transcript: ENST00000454954
  gene symbol: FOLR2
  hgvsc: ENST00000454954.2:c.94T>C
  hgvsp: ENSP00000414094.2:p.Ser32Pro
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000441547
  ensembl transcript: ENST00000539412
  gene symbol: FOLR2
  hgvsc: ENST00000539412.1:c.250T>C
  hgvsp: ENSP00000441547.1:p.Ser84Pro
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000298223
  ensembl transcript: ENST00000298223
  gene symbol: FOLR2
  hgvsc: ENST00000298223.6:c.217T>C
  hgvsp: ENSP00000298223.6:p.Ser73Pro
  variant of: http://identifiers.org/hgnc/3793
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165457
  ensembl protein: ENSP00000438568
  ensembl transcript: ENST00000536778
  gene symbol: FOLR2
  hgvsc: ENST00000536778.1:c.262T>C
  hgvsp: ENSP00000438568.1:p.Ser88Pro
  variant of: http://identifiers.org/hgnc/3793
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 10544
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19155
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 1.25e1
  variant carriers: 1
hgvs: p.Ser73Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ

GenotypeQuality
all individuals: 330
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2061
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1696
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 38531
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61138
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.435460301997078e-4
allele num: 8212
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8188
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

QD
type: SiteQuality
SIO_000300: 1.241e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.632e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-1

DP
type: SiteQuality
SIO_000300: 1.597178e6

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: -9.638e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.57e0

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 356
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8773
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1690
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 8.826125330979699e-5
allele num: 11330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8204
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61080
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8176
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16204
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.557e1

VQSLOD
type: SiteQuality
SIO_000300: -1.032e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.673e0

QD
type: SiteQuality
SIO_000300: 1.752e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

DP
type: SiteQuality
SIO_000300: 1.591908e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.427e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.080000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.47e-1

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

GenotypeQuality
all individuals: 1671
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1682
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 356
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8757
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61024
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.172077521293668e-5
allele num: 16202
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8168
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11328
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.15e0

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

MQ
type: SiteQuality
SIO_000300: 4.941e1

QD
type: SiteQuality
SIO_000300: 8.33e0

DP
type: SiteQuality
SIO_000300: 1.588268e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.041e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -7.8e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.76e0

GenotypeQuality
all individuals: 1619
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1982
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37626
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2040
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1668
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2247
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 2.44140625e-4
allele num: 8192
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16202
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60848
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.387e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.72e-1

QD
type: SiteQuality
SIO_000300: 1.48e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-2

FS
type: SiteQuality
SIO_000300: 2.054e0

DP
type: SiteQuality
SIO_000300: 1.574657e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.24e0

MQ
type: SiteQuality
SIO_000300: 5.357e1

GenotypeQuality
all individuals: 1668
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 2247
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1619
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 37626
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2040
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11310
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.220703125e-4
allele num: 8192
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.172077521293668e-5
allele num: 16202
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

East Asian
type: Population
allele count: 11
allele frequency: 1.348369698455504e-3
allele num: 8158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60848
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

MQ
type: SiteQuality
SIO_000300: 5.357e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.72e-1

QD
type: SiteQuality
SIO_000300: 1.48e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.24e0

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

FS
type: SiteQuality
SIO_000300: 2.054e0

DP
type: SiteQuality
SIO_000300: 1.574657e6

VQSLOD
type: SiteQuality
SIO_000300: -1.387e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-2

GenotypeQuality
all individuals: 198
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2333
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1647
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 157
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2019
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8144
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8170
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.650927821435647e-5
allele num: 60572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16188
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.603e1

MQ
type: SiteQuality
SIO_000300: 5.611e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.446e0

MQRankSum
type: SiteQuality
SIO_000300: -9.419999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.841e-1

DP
type: SiteQuality
SIO_000300: 1.556558e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.9e0

GenotypeQuality
all individuals: 36325
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2184
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 5.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60284
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11284
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.19041723412158e-5
allele num: 16154
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8136
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

FS
type: SiteQuality
SIO_000300: 1.2894e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.54e-1

DP
type: SiteQuality
SIO_000300: 1.540841e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.311e0

MQ
type: SiteQuality
SIO_000300: 5.354e1

QD
type: SiteQuality
SIO_000300: 2.83e0

GenotypeQuality
all individuals: 249
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1617
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1985
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36325
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11284
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.658814942605003e-5
allele num: 60284
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8136
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16154
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.24e-1

DP
type: SiteQuality
SIO_000300: 1.540841e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

MQ
type: SiteQuality
SIO_000300: 5.354e1

FS
type: SiteQuality
SIO_000300: 1.2894e1

MQRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.311e0

QD
type: SiteQuality
SIO_000300: 2.83e0

GenotypeQuality
all individuals: 1593
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35618
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2681
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.00150045013504e-5
allele num: 59982
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11250
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16156
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 9.26e-1

QD
type: SiteQuality
SIO_000300: 2.944e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.527596e6

MQRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.85e-1

MQ
type: SiteQuality
SIO_000300: 5.189e1

VQSLOD
type: SiteQuality
SIO_000300: 4.3e-1

GenotypeQuality
all individuals: 470
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2775
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8130
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11244
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8100
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60018
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8128
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.237930180737806e-4
allele num: 16156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.525114e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

QD
type: SiteQuality
SIO_000300: 1.374e1

MQ
type: SiteQuality
SIO_000300: 5.544e1

FS
type: SiteQuality
SIO_000300: 1.1367e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.649e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.22e-1

GenotypeQuality
all individuals: 1617
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 248
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1937
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.343698799612131e-5
allele num: 59814
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11232
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8072
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.062e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.7e0

QD
type: SiteQuality
SIO_000300: 1.642e1

DP
type: SiteQuality
SIO_000300: 1.517368e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

MQ
type: SiteQuality
SIO_000300: 5.085e1

MQRankSum
type: SiteQuality
SIO_000300: 9.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.39e-1

GenotypeQuality
all individuals: 511
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 7.25e1
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GenotypeQuality
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variant carriers: 4

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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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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variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10880
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4416
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4002
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3744
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 6.195786864931846e-4
allele num: 6456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36250
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.479e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

DP
type: SiteQuality
SIO_000300: 8.97198e5

MQRankSum
type: SiteQuality
SIO_000300: -1.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.523e0

QD
type: SiteQuality
SIO_000300: 1.476e1

VQSLOD
type: SiteQuality
SIO_000300: 2.22e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.9e-2

GenotypeQuality
all individuals: 25729
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1876
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variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 888
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variant carriers: 0

GenotypeQuality
all individuals: 3142
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 964
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 605
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 377
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 2.355157795572303e-4
allele num: 4246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37258
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4576
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3834
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10992
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 9.13808e5

VQSLOD
type: SiteQuality
SIO_000300: -2.715e0

QD
type: SiteQuality
SIO_000300: 2.55e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.56e-1

GenotypeQuality
all individuals: 647
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1927
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
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variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.5e0
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GenotypeQuality
all individuals: 787
bin: 7.5e0
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GenotypeQuality
all individuals: 964
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 377
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
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GenotypeQuality
all individuals: 336
bin: 5.75e1
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GenotypeQuality
all individuals: 25414
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variant carriers: 0

GenotypeQuality
all individuals: 19303
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11088
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3896
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4722
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.502403846153846e-4
allele num: 6656
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38056
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.794e0

QD
type: SiteQuality
SIO_000300: 7.84e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.37e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.584e-1

DP
type: SiteQuality
SIO_000300: 9.24202e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 431
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 162
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22467
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1466
bin: 9.75e1
variant carriers: 524

GenotypeQuality
all individuals: 22503
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 231
bin: 9.25e1
variant carriers: 11

GenotypeQuality
all individuals: 692
bin: 5.25e1
variant carriers: 5

GenotypeQuality
all individuals: 2058
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1224
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 7.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2711
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 7.25e1
variant carriers: 5

GenotypeQuality
all individuals: 601
bin: 5.75e1
variant carriers: 4

GenotypeQuality
all individuals: 378
bin: 8.25e1
variant carriers: 3

African
type: Population
allele count: 11
allele frequency: 1.546681664791901e-3
allele num: 7112
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 8.653513326410523e-4
allele num: 11556
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5212
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 464
allele frequency: 1.107134335480792e-2
allele num: 41910
num of homozygotes: 2

Latino
type: Population
allele count: 34
allele frequency: 6.640625e-3
allele num: 5120
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 35
allele frequency: 8.329366968110423e-3
allele num: 4202
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.37e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.61e0

QD
type: SiteQuality
SIO_000300: 1.386e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.4e-2

DP
type: SiteQuality
SIO_000300: 9.88552e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 137
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
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GenotypeQuality
all individuals: 433
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variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 6.75e1
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GenotypeQuality
all individuals: 179
bin: 1.25e1
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GenotypeQuality
all individuals: 985
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 497
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GenotypeQuality
all individuals: 221
bin: 8.75e1
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GenotypeQuality
all individuals: 637
bin: 7.75e1
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GenotypeQuality
all individuals: 21864
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5320
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.561643835616438e-5
allele num: 11680
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7238
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.866368047779022e-4
allele num: 5358
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4280
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 9.337940050424876e-5
allele num: 42836
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.303e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

DP
type: SiteQuality
SIO_000300: 1.00076e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

FS
type: SiteQuality
SIO_000300: 4.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.56e-1

GenotypeQuality
all individuals: 1251
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 2.5e0
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GenotypeQuality
all individuals: 985
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2647
bin: 2.75e1
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GenotypeQuality
all individuals: 353
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 7.25e1
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GenotypeQuality
all individuals: 614
bin: 4.75e1
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GenotypeQuality
all individuals: 734
bin: 5.25e1
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GenotypeQuality
all individuals: 23721
bin: 6.25e1
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GenotypeQuality
all individuals: 498
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GenotypeQuality
all individuals: 497
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4280
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.381597126277977e-4
allele num: 7238
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5320
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 5.599104143337066e-4
allele num: 5358
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11680
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42836
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.0e-1

QD
type: SiteQuality
SIO_000300: 1.303e1

VQSLOD
type: SiteQuality
SIO_000300: 1.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.00076e6

FS
type: SiteQuality
SIO_000300: 4.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.86e-1

GenotypeQuality
all individuals: 420
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1824
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16312
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 980
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 705
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50058
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7068
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.550387596899225e-4
allele num: 6450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8136
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.865345288658172e-5
allele num: 12714
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4802
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 712
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.8e-2

QD
type: SiteQuality
SIO_000300: 1.257e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

DP
type: SiteQuality
SIO_000300: 1.114918e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.68e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.45e-1

GenotypeQuality
all individuals: 711
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1503
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14041
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2627
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 33271
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 799
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6860
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 738
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.585983966899405e-4
allele num: 7734
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52718
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5034
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.158132e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.085e1

VQSLOD
type: SiteQuality
SIO_000300: 1.3e-2

GenotypeQuality
all individuals: 1930
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1633
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35062
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2878
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11226
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8120
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59738
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 7.449714427613609e-4
allele num: 8054
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.648e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.098e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.76e-1

MQ
type: SiteQuality
SIO_000300: 5.076e1

QD
type: SiteQuality
SIO_000300: 1.369e1

DP
type: SiteQuality
SIO_000300: 1.513729e6

GenotypeQuality
all individuals: 180
bin: 1.75e1
variant carriers: 9

GenotypeQuality
all individuals: 694
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7672
bin: 6.75e1
variant carriers: 3

GenotypeQuality
all individuals: 705
bin: 8.25e1
variant carriers: 10

GenotypeQuality
all individuals: 1779
bin: 7.75e1
variant carriers: 8

GenotypeQuality
all individuals: 2725
bin: 9.75e1
variant carriers: 2501

GenotypeQuality
all individuals: 706
bin: 3.25e1
variant carriers: 6

GenotypeQuality
all individuals: 190
bin: 9.25e1
variant carriers: 8

GenotypeQuality
all individuals: 323
bin: 4.25e1
variant carriers: 3

European (Finnish)
type: Population
allele count: 221
allele frequency: 3.426356589147287e-2
allele num: 6450
num of homozygotes: 4

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1564
allele frequency: 2.630870676894092e-2
allele num: 59448
num of homozygotes: 23

African
type: Population
allele count: 591
allele frequency: 7.374594459695533e-2
allele num: 8014
num of homozygotes: 19

Latino
type: Population
allele count: 120
allele frequency: 1.072194424588992e-2
allele num: 11192
num of homozygotes: 1

South Asian
type: Population
allele count: 59
allele frequency: 3.668241730912708e-3
allele num: 16084
num of homozygotes: 1

Other
type: Population
allele count: 25
allele frequency: 3.078817733990148e-2
allele num: 812
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.16e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.189e0

MQ
type: SiteQuality
SIO_000300: 5.084e1

DP
type: SiteQuality
SIO_000300: 1.501123e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

QD
type: SiteQuality
SIO_000300: 1.415e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e-1

GenotypeQuality
all individuals: 423
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1155
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 899
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 486
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 807
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9576
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1277
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2981
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38287
bin: 6.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9142
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.708583925642427e-5
allele num: 58528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14248
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7638
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.714e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.79e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.628e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.52e0

MQRankSum
type: SiteQuality
SIO_000300: 4.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 1.254289e6

QD
type: SiteQuality
SIO_000300: 5.5e0

GenotypeQuality
all individuals: 2982
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 67
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 899
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1340
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 220
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9546
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37878
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14324
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9156
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7662
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.406342609939707e-5
allele num: 58714
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

QD
type: SiteQuality
SIO_000300: 1.389e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.603e0

DP
type: SiteQuality
SIO_000300: 1.256065e6

VQSLOD
type: SiteQuality
SIO_000300: 8.46e-1

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37650
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2983
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 82
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1044
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9574
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 894
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1245
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1094
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58740
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5646
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 5.579578741804993e-4
allele num: 14338
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9162
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9328
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.07e-1

FS
type: SiteQuality
SIO_000300: 1.566e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.449999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

DP
type: SiteQuality
SIO_000300: 1.25547e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.51e-1

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

GenotypeQuality
all individuals: 410
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1447
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1239
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9995
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2927
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1206
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1538
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.964758322886195e-5
allele num: 14358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7660
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9292
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9166
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5676
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58722
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.248302e6

MQRankSum
type: SiteQuality
SIO_000300: -4.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.27e-1

FS
type: SiteQuality
SIO_000300: 2.146e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.062e0

VQSLOD
type: SiteQuality
SIO_000300: 9.389999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.46e-1

QD
type: SiteQuality
SIO_000300: 1.157e1

GenotypeQuality
all individuals: 91
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2854
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1527
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1806
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1489
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1033
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1932
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33117
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 987
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 843
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7650
num of homozygotes: 0

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

Latino
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allele count: 1
allele frequency: 1.08483402039488e-4
allele num: 9218
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5674
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 10
allele frequency: 1.705146131023429e-4
allele num: 58646
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.971e1

ReadPosRankSum
type: SiteQuality
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.093e0

GenotypeQuality
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variant carriers: 0

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5660
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.70456482460028e-5
allele num: 58666
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58630
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.36e-1

QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQRankSum
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FS
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DP
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MQ
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.44e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

Other
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allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14216
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9060
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.433712186244549e-5
allele num: 58246
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9110
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5634
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7558
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.18e-1

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.806e0

ClippingRankSum
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SIO_000300: -1.482e0

DP
type: SiteQuality
SIO_000300: 1.21599e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.376e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 1.723365387929549e-5
allele num: 58026
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9010
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7524
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5628
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9020
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.779999999999999e0

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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InbreedingCoeff
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DP
type: SiteQuality
SIO_000300: 1.2073e6

MQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.727593117269021e-5
allele num: 57884
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
allele num: 9022
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

QD
type: SiteQuality
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VQSLOD
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MQ
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
type: SiteQuality
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DP
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ClippingRankSum
type: SiteQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

European (Non-Finnish)
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allele num: 57924
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African
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East Asian
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Other
type: Population
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Latino
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South Asian
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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FS
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ClippingRankSum
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VQSLOD
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DP
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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European (Finnish)
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Other
type: Population
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East Asian
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Latino
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South Asian
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DP
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MQRankSum
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BaseQRankSum
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MQ
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FS
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QD
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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African
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allele frequency: 1.68123739071957e-3
allele num: 8922
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European (Non-Finnish)
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Latino
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allele frequency: 2.240645305848084e-4
allele num: 8926
num of homozygotes: 0

European (Finnish)
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South Asian
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allele frequency: 7.075137965190322e-5
allele num: 14134
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.202725e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.14e-1

QD
type: SiteQuality
SIO_000300: 1.251e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2.25e1
variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5518
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.502258957027283e-5
allele num: 57106
num of homozygotes: 0

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

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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MQRankSum
type: SiteQuality
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DP
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SIO_000300: 1.190595e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.31e-1

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

European (Finnish)
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
allele num: 8834
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.751129478513641e-5
allele num: 57106
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.86e-1

DP
type: SiteQuality
SIO_000300: 1.190595e6

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

South Asian
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allele frequency: 0.0e0
allele num: 13534
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.427347987439338e-4
allele num: 7006
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8172
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54456
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 760
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5306
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.713e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.67e-1

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.95e-1

MQ
type: SiteQuality
SIO_000300: 5.924e1

DP
type: SiteQuality
SIO_000300: 1.135226e6

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 54180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8112
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.433075379764976e-4
allele num: 6978
num of homozygotes: 0

African
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: 756
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5266
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.223e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.128113e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.682e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.78e0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.961399654793661e-5
allele num: 50984
num of homozygotes: 0

African
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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
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num of homozygotes: 0

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

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

African
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allele frequency: 7.84313725490196e-4
allele num: 7650
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 6.245836109260493e-5
allele num: 48032
num of homozygotes: 0

South Asian
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allele frequency: 1.595659805329504e-4
allele num: 12534
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Other
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East Asian
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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MQ
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MQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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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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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
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allele frequency: 2.089864158829676e-5
allele num: 47850
num of homozygotes: 0

European (Finnish)
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East Asian
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South Asian
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allele frequency: 7.979572294924992e-5
allele num: 12532
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Latino
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allele frequency: 4.497751124437781e-4
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African
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allele frequency: 1.18172268907563e-3
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Other
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QD
type: SiteQuality
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MQRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 6016
num of homozygotes: 0

South Asian
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allele frequency: 7.979572294924992e-5
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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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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Other
type: Population
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BaseQRankSum
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DP
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QD
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VQSLOD
type: SiteQuality
SIO_000300: 3.71e0

FS
type: SiteQuality
SIO_000300: 6.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

GenotypeQuality
all individuals: 128
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
all individuals: 559
bin: 7.75e1
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GenotypeQuality
all individuals: 1665
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
all individuals: 14942
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3919
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 687
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3898
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5972
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.216029343564231e-5
allele num: 47438
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12436
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4716
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

VQSLOD
type: SiteQuality
SIO_000300: 7.88e-1

DP
type: SiteQuality
SIO_000300: 9.41211e5

ClippingRankSum
type: SiteQuality
SIO_000300: 5.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

QD
type: SiteQuality
SIO_000300: 7.75e0

GenotypeQuality
all individuals: 3912
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7530
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5956
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.531393568147014e-4
allele num: 6530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12436
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.64e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

DP
type: SiteQuality
SIO_000300: 9.40314e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.621e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.718e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1016
bin: 9.75e1
variant carriers: 51

GenotypeQuality
all individuals: 3920
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 3873
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 9.25e1
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GenotypeQuality
all individuals: 580
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variant carriers: 0

GenotypeQuality
all individuals: 1662
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 131
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1421
bin: 7.5e0
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GenotypeQuality
all individuals: 262
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 726
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15423
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 51
allele frequency: 6.771109930961232e-3
allele num: 7532
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5886
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4700
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.538461538461539e-4
allele num: 6500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

QD
type: SiteQuality
SIO_000300: 1.351e1

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.37301e5

VQSLOD
type: SiteQuality
SIO_000300: 5.62e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1471
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8815
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26926
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variant carriers: 0

GenotypeQuality
all individuals: 466
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variant carriers: 0

GenotypeQuality
all individuals: 210
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variant carriers: 0

GenotypeQuality
all individuals: 3812
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GenotypeQuality
all individuals: 330
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variant carriers: 0

GenotypeQuality
all individuals: 986
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variant carriers: 1

GenotypeQuality
all individuals: 203
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GenotypeQuality
all individuals: 502
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GenotypeQuality
all individuals: 4753
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 500
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1501
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6916
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.566044200788077e-5
allele num: 11674
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43070
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5298
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5572
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.63e-1

FS
type: SiteQuality
SIO_000300: 4.472e0

QD
type: SiteQuality
SIO_000300: 1.619e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.67e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 8.29288e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

GenotypeQuality
all individuals: 218
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5504
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25795
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variant carriers: 0

GenotypeQuality
all individuals: 293
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variant carriers: 0

GenotypeQuality
all individuals: 4374
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GenotypeQuality
all individuals: 291
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GenotypeQuality
all individuals: 201
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variant carriers: 1

GenotypeQuality
all individuals: 491
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variant carriers: 3

GenotypeQuality
all individuals: 4796
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1945
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variant carriers: 0

GenotypeQuality
all individuals: 324
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variant carriers: 0

GenotypeQuality
all individuals: 1003
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 1264
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

African
type: Population
allele count: 17
allele frequency: 2.505896226415094e-3
allele num: 6784
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4262
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5106
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.14319729510929e-5
allele num: 41998
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.12846e5

QD
type: SiteQuality
SIO_000300: 1.261e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

GenotypeQuality
all individuals: 5609
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2329
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1213
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5022
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 485
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variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 419
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variant carriers: 0

GenotypeQuality
all individuals: 2869
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 486
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variant carriers: 0

GenotypeQuality
all individuals: 6671
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2509
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 127
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 736
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5026
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40662
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.068680182043856e-4
allele num: 4834
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.93179e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.19e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.428e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 5.766e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.308e0

MQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

GenotypeQuality
all individuals: 204
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 157
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variant carriers: 0

GenotypeQuality
all individuals: 1608
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variant carriers: 0

GenotypeQuality
all individuals: 4492
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variant carriers: 0

GenotypeQuality
all individuals: 414
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1602
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5683
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3770
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15898
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.004141905276428e-5
allele num: 11106
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64004
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.385e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

QD
type: SiteQuality
SIO_000300: 1.357e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.677e0

DP
type: SiteQuality
SIO_000300: 1.328931e6

VQSLOD
type: SiteQuality
SIO_000300: 8.05e-1

GenotypeQuality
all individuals: 63
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2785
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 969
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 395
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2225
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3097
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29126
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1534
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3671
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9774
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64006
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.5004500450045e-4
allele num: 11110
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8318
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.942e0

DP
type: SiteQuality
SIO_000300: 1.343731e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

QD
type: SiteQuality
SIO_000300: 1.306e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQ
type: SiteQuality
SIO_000300: 5.836e1

VQSLOD
type: SiteQuality
SIO_000300: -1.57e0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

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

GenotypeQuality
all individuals: 2227
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1960
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30455
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3568
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.5e0
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GenotypeQuality
all individuals: 2043
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1622
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5917
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6462
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.560890331845285e-5
allele num: 64066
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15916
num of homozygotes: 0

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

Latino
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allele count: 2
allele frequency: 1.797914419273643e-4
allele num: 11124
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -5.688e0

DP
type: SiteQuality
SIO_000300: 1.355828e6

BaseQRankSum
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SIO_000300: -9.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

FS
type: SiteQuality
SIO_000300: 3.1366e1

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

QD
type: SiteQuality
SIO_000300: 1.234e1

MQRankSum
type: SiteQuality
SIO_000300: -3.1e-2

GenotypeQuality
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bin: 7.25e1
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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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11142
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15948
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6474
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9818
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.556904873112253e-5
allele num: 64230
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8376
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.511e0

MQRankSum
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 2.772e0

QD
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ClippingRankSum
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SIO_000300: 1.21e0

InbreedingCoeff
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SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.382259e6

GenotypeQuality
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variant carriers: 2

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

Other
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allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15970
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.792435920415845e-4
allele num: 11158
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8374
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64282
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.387e0

DP
type: SiteQuality
SIO_000300: 1.407372e6

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.256e0

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

MQ
type: SiteQuality
SIO_000300: 5.67e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.71e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.411e-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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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545117428924598e-5
allele num: 64720
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16074
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9932
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11246
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.453552e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.12e0

QD
type: SiteQuality
SIO_000300: 1.457e1

MQ
type: SiteQuality
SIO_000300: 5.696e1

MQRankSum
type: SiteQuality
SIO_000300: 8.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.228e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.473e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16098
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544115376300917e-5
allele num: 64762
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11252
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9944
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.22e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.383e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.35e-1

QD
type: SiteQuality
SIO_000300: 2.428e1

FS
type: SiteQuality
SIO_000300: 2.541e0

MQ
type: SiteQuality
SIO_000300: 5.901e1

DP
type: SiteQuality
SIO_000300: 1.458976e6

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 3
allele frequency: 2.645036148827367e-4
allele num: 11342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10056
num of homozygotes: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.072731173567904e-4
allele num: 65254
num of homozygotes: 0

South Asian
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allele count: 6
allele frequency: 3.699593044765076e-4
allele num: 16218
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 888
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FS
type: SiteQuality
SIO_000300: 7.56e-1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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QD
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65316
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8520
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South Asian
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allele count: 1
allele frequency: 6.162188809465122e-5
allele num: 16228
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
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FS
type: SiteQuality
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DP
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QD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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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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BaseQRankSum
type: SiteQuality
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DP
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MQ
type: SiteQuality
SIO_000300: 5.896e1

MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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FS
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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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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: 7
allele frequency: 4.261536588335566e-4
allele num: 16426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6592
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.547521600727603e-5
allele num: 65970
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 896
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VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
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SIO_000300: 4.373e0

MQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 7.75e-1

QD
type: SiteQuality
SIO_000300: 1.595e1

MQ
type: SiteQuality
SIO_000300: 5.608e1

DP
type: SiteQuality
SIO_000300: 1.532666e6

GenotypeQuality
all individuals: 1168
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2244
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7839
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10236
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.517450682852807e-4
allele num: 6590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65974
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.484e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

DP
type: SiteQuality
SIO_000300: 1.532234e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.511e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.28e-1

QD
type: SiteQuality
SIO_000300: 1.238e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.19e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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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: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 209
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514830187535977e-5
allele num: 66014
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.714e1

QD
type: SiteQuality
SIO_000300: 1.088e1

FS
type: SiteQuality
SIO_000300: 2.422e0

DP
type: SiteQuality
SIO_000300: 1.53449e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

VQSLOD
type: SiteQuality
SIO_000300: -1.244e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.33e-1

GenotypeQuality
all individuals: 815
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 9

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 452
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variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.469794578825817e-4
allele num: 16454
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65952
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.222e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.897e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

DP
type: SiteQuality
SIO_000300: 1.535643e6

VQSLOD
type: SiteQuality
SIO_000300: 1.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.86e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.443e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1277
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1005
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65952
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10252
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.077549532028686e-5
allele num: 16454
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.44e-1

DP
type: SiteQuality
SIO_000300: 1.535643e6

QD
type: SiteQuality
SIO_000300: 1.222e1

VQSLOD
type: SiteQuality
SIO_000300: 1.56e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.443e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.04e-1

MQ
type: SiteQuality
SIO_000300: 5.897e1

GenotypeQuality
all individuals: 49
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2094
bin: 7.75e1
variant carriers: 7

GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 1144
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variant carriers: 2

GenotypeQuality
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variant carriers: 6

GenotypeQuality
all individuals: 502
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variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 5.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.076810889645114e-5
allele num: 16456
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

African
type: Population
allele count: 34
allele frequency: 3.355704697986577e-3
allele num: 10132
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 18
allele frequency: 2.733070148800486e-4
allele num: 65860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-2

QD
type: SiteQuality
SIO_000300: 8.8e-1

FS
type: SiteQuality
SIO_000300: 6.755500000000001e1

DP
type: SiteQuality
SIO_000300: 1.538671e6

MQ
type: SiteQuality
SIO_000300: 5.567e1

VQSLOD
type: SiteQuality
SIO_000300: -2.332e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.393e0

MQRankSum
type: SiteQuality
SIO_000300: -3.476e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 997
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variant carriers: 1

GenotypeQuality
all individuals: 2236
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GenotypeQuality
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GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 478
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GenotypeQuality
all individuals: 975
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 353
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 579
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GenotypeQuality
all individuals: 1165
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 41263
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variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515702679762338e-5
allele num: 65976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -3.564e0

DP
type: SiteQuality
SIO_000300: 1.536197e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.72e-1

FS
type: SiteQuality
SIO_000300: 2.003e0

MQRankSum
type: SiteQuality
SIO_000300: -2.898e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.721e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.72e-1

QD
type: SiteQuality
SIO_000300: 5.75e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 432
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 7
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GenotypeQuality
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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: 456
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GenotypeQuality
all individuals: 7647
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515564851019975e-5
allele num: 65982
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.02e-1

DP
type: SiteQuality
SIO_000300: 1.540526e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.761e0

FS
type: SiteQuality
SIO_000300: 4.058e0

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.24e-1

QD
type: SiteQuality
SIO_000300: 7.83e0

MQ
type: SiteQuality
SIO_000300: 5.039e1

GenotypeQuality
all individuals: 988
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7648
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2258
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GenotypeQuality
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GenotypeQuality
all individuals: 493
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GenotypeQuality
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GenotypeQuality
all individuals: 51
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GenotypeQuality
all individuals: 275
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1031
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GenotypeQuality
all individuals: 310
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GenotypeQuality
all individuals: 458
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GenotypeQuality
all individuals: 527
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65996
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: -4.11e-1

MQ
type: SiteQuality
SIO_000300: 5.75e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.295e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

DP
type: SiteQuality
SIO_000300: 1.540467e6

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

GenotypeQuality
all individuals: 7646
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 4.25e1
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GenotypeQuality
all individuals: 503
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41349
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2183
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2258
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 341
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515472979116782e-5
allele num: 65986
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.736714136853074e-4
allele num: 11516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.291e1

MQRankSum
type: SiteQuality
SIO_000300: -6.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.087e0

FS
type: SiteQuality
SIO_000300: 6.870000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.024e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.99e-1

MQ
type: SiteQuality
SIO_000300: 5.875e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

DP
type: SiteQuality
SIO_000300: 1.539023e6

GenotypeQuality
all individuals: 2470
bin: 3.75e1
variant carriers: 52

GenotypeQuality
all individuals: 2865
bin: 5.25e1
variant carriers: 37

GenotypeQuality
all individuals: 1216
bin: 1.25e1
variant carriers: 22

GenotypeQuality
all individuals: 1526
bin: 1.75e1
variant carriers: 36

GenotypeQuality
all individuals: 2864
bin: 4.75e1
variant carriers: 43

GenotypeQuality
all individuals: 260
bin: 8.25e1
variant carriers: 27

GenotypeQuality
all individuals: 1962
bin: 2.75e1
variant carriers: 42

GenotypeQuality
all individuals: 3766
bin: 6.75e1
variant carriers: 41

GenotypeQuality
all individuals: 2428
bin: 5.75e1
variant carriers: 41

GenotypeQuality
all individuals: 1115
bin: 7.5e0
variant carriers: 30

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 28

GenotypeQuality
all individuals: 459
bin: 9.75e1
variant carriers: 209

GenotypeQuality
all individuals: 26542
bin: 6.25e1
variant carriers: 46

GenotypeQuality
all individuals: 579
bin: 7.75e1
variant carriers: 36

GenotypeQuality
all individuals: 732
bin: 7.25e1
variant carriers: 33

GenotypeQuality
all individuals: 112
bin: 9.25e1
variant carriers: 18

Latino
type: Population
allele count: 61
allele frequency: 6.187867721647393e-3
allele num: 9858
num of homozygotes: 0

South Asian
type: Population
allele count: 25
allele frequency: 1.631002087682672e-3
allele num: 15328
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 361
allele frequency: 7.07843137254902e-2
allele num: 5100
num of homozygotes: 0

African
type: Population
allele count: 20
allele frequency: 2.154708037060978e-3
allele num: 9282
num of homozygotes: 0

Other
type: Population
allele count: 11
allele frequency: 1.41025641025641e-2
allele num: 780
num of homozygotes: 0

East Asian
type: Population
allele count: 41
allele frequency: 5.452127659574468e-3
allele num: 7520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 274
allele frequency: 4.92929874428813e-3
allele num: 55586
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.868e1

VQSLOD
type: SiteQuality
SIO_000300: -3.194e2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.74e-2

QD
type: SiteQuality
SIO_000300: 9.399999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.82e-1

FS
type: SiteQuality
SIO_000300: 2.66032e2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.169e0

DP
type: SiteQuality
SIO_000300: 1.67678e6

GenotypeQuality
all individuals: 113
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 1431
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1019
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42232
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 204
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 797
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 719
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1138
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1179
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 978
bin: 2.25e1
variant carriers: 1

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

GenotypeQuality
all individuals: 1085
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 3.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525087692542321e-5
allele num: 65570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.275494195167869e-4
allele num: 6374
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.44e0

DP
type: SiteQuality
SIO_000300: 1.606499e6

QD
type: SiteQuality
SIO_000300: 4.3e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.49e2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.269e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

FS
type: SiteQuality
SIO_000300: 1.79333e2

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

MQ
type: SiteQuality
SIO_000300: 5.895e1