22-30057172-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057172
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057172
    reference: chr 22
allele count: 1
allele frequency: 8.250280509537325e-6
allele num: 121208
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.199-22G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+18898G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.676-22G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.676-22G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.553-22G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.676-22G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.427-22G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.550-22G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.676-22G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.427-22G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.676-22G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.199-22G>A
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4954
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

22-30057174-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057174
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057174
    reference: chr 22
allele count: 3
allele frequency: 2.474920802534319e-5
allele num: 121216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.676-20T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.199-20T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.676-20T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.427-20T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.676-20T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.553-20T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.427-20T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.199-20T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.550-20T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.676-20T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.676-20T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+18900T>C
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9337
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4954
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

22-30057185-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057185
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057185
    reference: chr 22
allele count: 3
allele frequency: 2.473492406378312e-5
allele num: 121286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+18911G>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.550-9G>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.553-9G>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.676-9G>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.199-9G>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.676-9G>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.676-9G>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.676-9G>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.199-9G>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.676-9G>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.427-9G>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.427-9G>T
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4954
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9336
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

22-30057201-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057201
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057201
    reference: chr 22
allele count: 2
allele frequency: 1.648070932972955e-5
allele num: 121354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+18927A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.206A>G
  hgvsp: ENSP00000335160.6:p.Lys69Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.683A>G
  hgvsp: ENSP00000344666.4:p.Lys228Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.560A>G
  hgvsp: ENSP00000354897.4:p.Lys187Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.557A>G
  hgvsp: ENSP00000355183.4:p.Lys186Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.683A>G
  hgvsp: ENSP00000380891.3:p.Lys228Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.683A>G
  hgvsp: ENSP00000384029.1:p.Lys228Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.206A>G
  hgvsp: ENSP00000395885.1:p.Lys69Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.683A>G
  hgvsp: ENSP00000384797.3:p.Lys228Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.683A>G
  hgvsp: ENSP00000354529.4:p.Lys228Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.434A>G
  hgvsp: ENSP00000340626.4:p.Lys145Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.434A>G
  hgvsp: ENSP00000335652.7:p.Lys145Arg
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5014
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5273
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4955
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9335
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys228Arg
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: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

22-30057209-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057209
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057209
    reference: chr 22
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.691G>C
  hgvsp: ENSP00000380891.3:p.Glu231Gln
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.214G>C
  hgvsp: ENSP00000335160.6:p.Glu72Gln
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.442G>C
  hgvsp: ENSP00000340626.4:p.Glu148Gln
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.565G>C
  hgvsp: ENSP00000355183.4:p.Glu189Gln
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.568G>C
  hgvsp: ENSP00000354897.4:p.Glu190Gln
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.442G>C
  hgvsp: ENSP00000335652.7:p.Glu148Gln
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.691G>C
  hgvsp: ENSP00000384029.1:p.Glu231Gln
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+18935G>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.214G>C
  hgvsp: ENSP00000395885.1:p.Glu72Gln
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.691G>C
  hgvsp: ENSP00000384797.3:p.Glu231Gln
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.691G>C
  hgvsp: ENSP00000344666.4:p.Glu231Gln
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.691G>C
  hgvsp: ENSP00000354529.4:p.Glu231Gln
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4955
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5014
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu231Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

22-30057217-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057217
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057217
    reference: chr 22
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.450G>T
  hgvsp: ENST00000353887.4:c.450G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.699G>T
  hgvsp: ENST00000403999.3:c.699G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.450G>T
  hgvsp: ENST00000334961.7:c.450G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.699G>T
  hgvsp: ENST00000403435.1:c.699G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.699G>T
  hgvsp: ENST00000361166.4:c.699G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.699G>T
  hgvsp: ENST00000397789.3:c.699G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.576G>T
  hgvsp: ENST00000361452.4:c.576G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.222G>T
  hgvsp: ENST00000347330.5:c.222G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.222G>T
  hgvsp: ENST00000432151.1:c.222G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+18943G>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.573G>T
  hgvsp: ENST00000361676.4:c.573G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.699G>T
  hgvsp: ENST00000338641.4:c.699G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5319
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4955
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9333
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu233Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/22-30057223-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057223
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057223
    reference: chr 22
allele count: 2
allele frequency: 1.64766361299677e-5
allele num: 121384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.582A>C
  hgvsp: ENST00000361452.4:c.582A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.579A>C
  hgvsp: ENST00000361676.4:c.579A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.705A>C
  hgvsp: ENST00000403435.1:c.705A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.228A>C
  hgvsp: ENST00000347330.5:c.228A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.228A>C
  hgvsp: ENST00000432151.1:c.228A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.705A>C
  hgvsp: ENST00000397789.3:c.705A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.456A>C
  hgvsp: ENST00000334961.7:c.456A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+18949A>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.705A>C
  hgvsp: ENST00000338641.4:c.705A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.705A>C
  hgvsp: ENST00000361166.4:c.705A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.456A>C
  hgvsp: ENST00000353887.4:c.456A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.705A>C
  hgvsp: ENST00000403999.3:c.705A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4955
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4524
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9331
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Gly235Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

22-30057238-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057238
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057238
    reference: chr 22
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.720G>T
  hgvsp: ENST00000403435.1:c.720G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.720G>T
  hgvsp: ENST00000403999.3:c.720G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+18964G>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.720G>T
  hgvsp: ENST00000397789.3:c.720G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.243G>T
  hgvsp: ENST00000347330.5:c.243G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.597G>T
  hgvsp: ENST00000361452.4:c.597G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.243G>T
  hgvsp: ENST00000432151.1:c.243G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.471G>T
  hgvsp: ENST00000334961.7:c.471G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.720G>T
  hgvsp: ENST00000361166.4:c.720G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.594G>T
  hgvsp: ENST00000361676.4:c.594G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.471G>T
  hgvsp: ENST00000353887.4:c.471G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.720G>T
  hgvsp: ENST00000338641.4:c.720G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5017
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4523
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly240Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

22-30057245-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057245
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057245
    reference: chr 22
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.478A>G
  hgvsp: ENSP00000340626.4:p.Ile160Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.727A>G
  hgvsp: ENSP00000384029.1:p.Ile243Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.727A>G
  hgvsp: ENSP00000354529.4:p.Ile243Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.604A>G
  hgvsp: ENSP00000354897.4:p.Ile202Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.727A>G
  hgvsp: ENSP00000384797.3:p.Ile243Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.478A>G
  hgvsp: ENSP00000335652.7:p.Ile160Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.727A>G
  hgvsp: ENSP00000380891.3:p.Ile243Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.727A>G
  hgvsp: ENSP00000344666.4:p.Ile243Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+18971A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.250A>G
  hgvsp: ENSP00000395885.1:p.Ile84Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.601A>G
  hgvsp: ENSP00000355183.4:p.Ile201Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.250A>G
  hgvsp: ENSP00000335160.6:p.Ile84Val
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9318
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile243Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

22-30057256-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057256
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057256
    reference: chr 22
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.261T>C
  hgvsp: ENST00000432151.1:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.738T>C
  hgvsp: ENST00000403435.1:c.738T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.615T>C
  hgvsp: ENST00000361452.4:c.615T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.738T>C
  hgvsp: ENST00000397789.3:c.738T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.738T>C
  hgvsp: ENST00000403999.3:c.738T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+18982T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.489T>C
  hgvsp: ENST00000353887.4:c.489T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.612T>C
  hgvsp: ENST00000361676.4:c.612T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.738T>C
  hgvsp: ENST00000361166.4:c.738T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.261T>C
  hgvsp: ENST00000347330.5:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.489T>C
  hgvsp: ENST00000334961.7:c.489T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.738T>C
  hgvsp: ENST00000338641.4:c.738T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5017
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro246Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

22-30057266-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057266
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057266
    reference: chr 22
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.748C>T
  hgvsp: ENST00000361166.4:c.748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.748C>T
  hgvsp: ENST00000403999.3:c.748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.499C>T
  hgvsp: ENST00000353887.4:c.499C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+18992C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.748C>T
  hgvsp: ENST00000403435.1:c.748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.625C>T
  hgvsp: ENST00000361452.4:c.625C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.271C>T
  hgvsp: ENST00000432151.1:c.271C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.748C>T
  hgvsp: ENST00000397789.3:c.748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.748C>T
  hgvsp: ENST00000338641.4:c.748C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.271C>T
  hgvsp: ENST00000347330.5:c.271C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.499C>T
  hgvsp: ENST00000334961.7:c.499C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.622C>T
  hgvsp: ENST00000361676.4:c.622C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5017
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu250Leu
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

22-30057276-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057276
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057276
    reference: chr 22
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.758A>G
  hgvsp: ENSP00000384797.3:p.Lys253Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.758A>G
  hgvsp: ENSP00000380891.3:p.Lys253Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.509A>G
  hgvsp: ENSP00000340626.4:p.Lys170Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+19002A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.758A>G
  hgvsp: ENSP00000384029.1:p.Lys253Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.281A>G
  hgvsp: ENSP00000395885.1:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.632A>G
  hgvsp: ENSP00000355183.4:p.Lys211Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.758A>G
  hgvsp: ENSP00000344666.4:p.Lys253Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.635A>G
  hgvsp: ENSP00000354897.4:p.Lys212Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.509A>G
  hgvsp: ENSP00000335652.7:p.Lys170Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.758A>G
  hgvsp: ENSP00000354529.4:p.Lys253Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.281A>G
  hgvsp: ENSP00000335160.6:p.Lys94Arg
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5018
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys253Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

22-30057277-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057277
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057277
    reference: chr 22
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.759G>A
  hgvsp: ENST00000338641.4:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.759G>A
  hgvsp: ENST00000403435.1:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.282G>A
  hgvsp: ENST00000432151.1:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.759G>A
  hgvsp: ENST00000361166.4:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.633G>A
  hgvsp: ENST00000361676.4:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.510G>A
  hgvsp: ENST00000353887.4:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.636G>A
  hgvsp: ENST00000361452.4:c.636G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.282G>A
  hgvsp: ENST00000347330.5:c.282G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+19003G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.510G>A
  hgvsp: ENST00000334961.7:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.759G>A
  hgvsp: ENST00000397789.3:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.759G>A
  hgvsp: ENST00000403999.3:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3823
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5018
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys253Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/22-30057280-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057280
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057280
    reference: chr 22
allele count: 2
allele frequency: 1.648098094798602e-5
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.636C>A
  hgvsp: ENST00000361676.4:c.636C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.639C>A
  hgvsp: ENST00000361452.4:c.639C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.285C>A
  hgvsp: ENST00000432151.1:c.285C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.762C>A
  hgvsp: ENST00000361166.4:c.762C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.762C>A
  hgvsp: ENST00000338641.4:c.762C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.762C>A
  hgvsp: ENST00000397789.3:c.762C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.285C>A
  hgvsp: ENST00000347330.5:c.285C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.513C>A
  hgvsp: ENST00000353887.4:c.513C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.513C>A
  hgvsp: ENST00000334961.7:c.513C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.762C>A
  hgvsp: ENST00000403999.3:c.762C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+19006C>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.762C>A
  hgvsp: ENST00000403435.1:c.762C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5273
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5018
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile254Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

22-30057288-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057288
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057288
    reference: chr 22
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.521C>T
  hgvsp: ENSP00000335652.7:p.Pro174Leu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.293C>T
  hgvsp: ENSP00000395885.1:p.Pro98Leu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.770C>T
  hgvsp: ENSP00000380891.3:p.Pro257Leu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.770C>T
  hgvsp: ENSP00000384029.1:p.Pro257Leu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.770C>T
  hgvsp: ENSP00000344666.4:p.Pro257Leu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.521C>T
  hgvsp: ENSP00000340626.4:p.Pro174Leu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.647C>T
  hgvsp: ENSP00000354897.4:p.Pro216Leu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.644C>T
  hgvsp: ENSP00000355183.4:p.Pro215Leu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.770C>T
  hgvsp: ENSP00000354529.4:p.Pro257Leu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.293C>T
  hgvsp: ENSP00000335160.6:p.Pro98Leu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+19014C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.770C>T
  hgvsp: ENSP00000384797.3:p.Pro257Leu
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5274
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4521
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5019
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro257Leu
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

22-30057289-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057289
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057289
    reference: chr 22
allele count: 2
allele frequency: 1.648315421639085e-5
allele num: 121336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.294G>A
  hgvsp: ENST00000432151.1:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.771G>A
  hgvsp: ENST00000403999.3:c.771G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.648G>A
  hgvsp: ENST00000361452.4:c.648G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.645G>A
  hgvsp: ENST00000361676.4:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.522G>A
  hgvsp: ENST00000353887.4:c.522G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.522G>A
  hgvsp: ENST00000334961.7:c.522G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.771G>A
  hgvsp: ENST00000361166.4:c.771G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.771G>A
  hgvsp: ENST00000403435.1:c.771G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.294G>A
  hgvsp: ENST00000347330.5:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.771G>A
  hgvsp: ENST00000338641.4:c.771G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.771G>A
  hgvsp: ENST00000397789.3:c.771G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+19015G>A
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9313
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4520
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro257Pro
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

22-30057301-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057301
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057301
    reference: chr 22
allele count: 9
allele frequency: 7.419498441905327e-5
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.306C>T
  hgvsp: ENST00000432151.1:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.657C>T
  hgvsp: ENST00000361676.4:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.783C>T
  hgvsp: ENST00000403435.1:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.783C>T
  hgvsp: ENST00000403999.3:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.783C>T
  hgvsp: ENST00000338641.4:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.534C>T
  hgvsp: ENST00000353887.4:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.783C>T
  hgvsp: ENST00000397789.3:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.660C>T
  hgvsp: ENST00000361452.4:c.660C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.783C>T
  hgvsp: ENST00000361166.4:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+19027C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.306C>T
  hgvsp: ENST00000347330.5:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.534C>T
  hgvsp: ENST00000334961.7:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4520
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5275
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile261Ile
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

22-30057313-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057313
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057313
    reference: chr 22
allele count: 2
allele frequency: 1.649675014022238e-5
allele num: 121236
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.318G>A
  hgvsp: ENST00000432151.1:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.672G>A
  hgvsp: ENST00000361452.4:c.672G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.669G>A
  hgvsp: ENST00000361676.4:c.669G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.795G>A
  hgvsp: ENST00000397789.3:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.795G>A
  hgvsp: ENST00000403999.3:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.795G>A
  hgvsp: ENST00000403435.1:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+19039G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.795G>A
  hgvsp: ENST00000361166.4:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.318G>A
  hgvsp: ENST00000347330.5:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.546G>A
  hgvsp: ENST00000353887.4:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.795G>A
  hgvsp: ENST00000338641.4:c.795G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.546G>A
  hgvsp: ENST00000334961.7:c.546G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4300
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9305
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser265Ser
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

22-30057334-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057334
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057334
    reference: chr 22
allele count: 1
allele frequency: 8.260230295220631e-6
allele num: 121062
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.687+6A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.333+6A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.561+6A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.333+6A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.810+6A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.810+6A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.684+6A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.810+6A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.810+6A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.561+6A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+19060A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.810+6A>G
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5277
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.810+6A>G
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

22-30057335-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057335
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057333
    reference: chr 22
allele count: 3
allele frequency: 2.478069088566189e-5
allele num: 121062
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.810+8_810+9delAT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.561+8_561+9delAT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.687+8_687+9delAT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.684+8_684+9delAT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.810+8_810+9delAT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.561+8_561+9delAT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.810+8_810+9delAT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.333+8_333+9delAT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.810+8_810+9delAT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.810+8_810+9delAT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.333+8_333+9delAT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+19062_447+19063delAT
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.810+8_810+9delAT
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: CAT
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

22-30057348-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057348
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057348
    reference: chr 22
allele count: 1
allele frequency: 8.26801600687899e-6
allele num: 120948
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.333+20C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+19074C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.687+20C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.333+20C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.810+20C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.810+20C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.810+20C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.810+20C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.810+20C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.561+20C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.561+20C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.684+20C>T
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4957
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

22-30057349-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057349
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057349
    reference: chr 22
allele count: 4
allele frequency: 3.307097030226867e-5
allele num: 120952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.687+21A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.810+21A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.810+21A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.810+21A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.684+21A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.810+21A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.561+21A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.810+21A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.333+21A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+19075A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.333+21A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.561+21A>G
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9301
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4957
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

22-30057349-AGAT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057349
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057346
    reference: chr 22
allele count: 5
allele frequency: 4.133871287783583e-5
allele num: 120952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.810+23_810+25delATG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.810+23_810+25delATG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.561+23_561+25delATG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.333+23_333+25delATG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.684+23_684+25delATG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.687+23_687+25delATG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.561+23_561+25delATG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+19077_447+19079delATG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.810+23_810+25delATG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.333+23_333+25delATG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.810+23_810+25delATG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.810+23_810+25delATG
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4957
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2611
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5020
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9301
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: AGAT
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

22-30057351-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057351
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057351
    reference: chr 22
allele count: 1
allele frequency: 8.268152729317216e-6
allele num: 120946
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.687+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.561+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.810+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.333+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.561+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.684+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.333+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.810+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.810+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.810+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+19077A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.810+23A>G
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4957
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD

22-30057374-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057374
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057374
    reference: chr 22
allele count: 9
allele frequency: 7.45489786789921e-5
allele num: 120726
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.810+46G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.687+46G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.684+46G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.561+46G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+19100G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.333+46G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.810+46G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.810+46G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.810+46G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.333+46G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.561+46G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.810+46G>A
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9299
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4304
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4957
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5327
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5019
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

22-30057379-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057379
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057379
    reference: chr 22
allele count: 2
allele frequency: 1.657605092162843e-5
allele num: 120656
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.810+51C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.810+51C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.333+51C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.684+51C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.810+51C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.561+51C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.810+51C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+19105C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.687+51C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.810+51C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.561+51C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.333+51C>T
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4523
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5017
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4302
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9298
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ

22-30057380-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30057380
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30057380
    reference: chr 22
allele count: 1
allele frequency: 8.286926544683108e-6
allele num: 120672
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.684+52C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.561+52C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.810+52C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.810+52C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.810+52C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.687+52C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+19106C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.333+52C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.810+52C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.333+52C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.810+52C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.561+52C>T
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4523
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5328
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9298
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP

22-30060933-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30060933
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30060933
    reference: chr 22
allele count: 1
allele frequency: 1.015352124116644e-5
allele num: 98488
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.811-46A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.334-46A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.334-46A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.811-46A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.685-46A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.811-46A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.811-46A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.688-46A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.811-46A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22659A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.562-46A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.562-46A>G
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19018
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP

22-30060938-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30060938
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30060937
    reference: chr 22
allele count: 1
allele frequency: 1.017894586836587e-5
allele num: 98242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.811-39delG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.562-39delG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.811-39delG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.334-39delG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.688-39delG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.562-39delG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.685-39delG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.811-39delG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.334-39delG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.811-39delG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.811-39delG
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22666delG
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18654
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8656
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: AG
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/22-30060945-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30060945
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30060945
    reference: chr 22
allele count: 1
allele frequency: 1.008471157724889e-5
allele num: 99160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.562-34C>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.562-34C>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.811-34C>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.334-34C>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.811-34C>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.811-34C>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.811-34C>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.334-34C>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.811-34C>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.688-34C>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22671C>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.685-34C>A
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17008
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6045
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9983
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

22-30060945-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30060945
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30060945
    reference: chr 22
allele count: 36
allele frequency: 3.630496167809601e-4
allele num: 99160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.562-34C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.685-34C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.811-34C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.811-34C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22671C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.688-34C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.811-34C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.811-34C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.334-34C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.562-34C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.811-34C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.334-34C>T
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6045
  bin: 1.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12712
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9983
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17008
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

22-30060949-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30060949
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30060949
    reference: chr 22
allele count: 1
allele frequency: 9.909035058166036e-6
allele num: 100918
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.562-30C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.688-30C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.811-30C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.811-30C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.334-30C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.811-30C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.685-30C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.334-30C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.811-30C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.562-30C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.811-30C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22675C>G
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9675
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-30060954-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30060954
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30060954
    reference: chr 22
allele count: 1
allele frequency: 9.75781112780781e-6
allele num: 102482
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22680A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.811-25A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.334-25A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.811-25A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.685-25A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.562-25A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.562-25A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.811-25A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.811-25A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.811-25A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.688-25A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.334-25A>G
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9098
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11840
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

22-30060955-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30060955
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30060953
    reference: chr 22
allele count: 1
allele frequency: 9.7431700378035e-6
allele num: 102636
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.562-20_562-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.811-20_811-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.334-20_334-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.811-20_811-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.811-20_811-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.334-20_334-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.685-20_685-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.688-20_688-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22685_447+22686delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.811-20_811-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.562-20_562-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.811-20_811-19delGT
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8980
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11503
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: CTG
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

22-30060962-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30060962
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30060962
    reference: chr 22
allele count: 24
allele frequency: 2.289770450512336e-4
allele num: 104814
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.811-17C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.811-17C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.811-17C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.685-17C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.334-17C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.562-17C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.688-17C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.334-17C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.811-17C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22688C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.811-17C>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.562-17C>G
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24949
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8970
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 3.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

22-30060967-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30060967
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30060967
    reference: chr 22
allele count: 1
allele frequency: 9.321923299215094e-6
allele num: 107274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.334-12T>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.811-12T>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.688-12T>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.811-12T>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.811-12T>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.562-12T>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.811-12T>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.811-12T>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.685-12T>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.562-12T>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22693T>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.334-12T>G
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6545
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6893
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD

22-30060969-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30060969
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30060969
    reference: chr 22
allele count: 1
allele frequency: 9.259773691130989e-6
allele num: 107994
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.811-10A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.562-10A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.688-10A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.811-10A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22695A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.685-10A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.334-10A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.811-10A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.334-10A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.811-10A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.562-10A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.811-10A>G
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

22-30060994-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30060994
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30060994
    reference: chr 22
allele count: 2
allele frequency: 1.738253750282466e-5
allele num: 115058
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.349C>T
  hgvsp: ENST00000432151.1:c.349C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.826C>T
  hgvsp: ENST00000338641.4:c.826C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.577C>T
  hgvsp: ENST00000334961.7:c.577C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.577C>T
  hgvsp: ENST00000353887.4:c.577C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.700C>T
  hgvsp: ENST00000361676.4:c.700C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.703C>T
  hgvsp: ENST00000361452.4:c.703C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.826C>T
  hgvsp: ENST00000403435.1:c.826C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22720C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.826C>T
  hgvsp: ENST00000397789.3:c.826C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.349C>T
  hgvsp: ENST00000347330.5:c.349C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.826C>T
  hgvsp: ENST00000361166.4:c.826C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.826C>T
  hgvsp: ENST00000403999.3:c.826C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2251
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu276Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

22-30060995-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30060995
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30060995
    reference: chr 22
allele count: 3
allele frequency: 2.601862933860644e-5
allele num: 115302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.578T>C
  hgvsp: ENSP00000340626.4:p.Leu193Pro
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.704T>C
  hgvsp: ENSP00000354897.4:p.Leu235Pro
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.701T>C
  hgvsp: ENSP00000355183.4:p.Leu234Pro
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.827T>C
  hgvsp: ENSP00000380891.3:p.Leu276Pro
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.350T>C
  hgvsp: ENSP00000335160.6:p.Leu117Pro
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.827T>C
  hgvsp: ENSP00000384029.1:p.Leu276Pro
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.827T>C
  hgvsp: ENSP00000344666.4:p.Leu276Pro
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22721T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.827T>C
  hgvsp: ENSP00000354529.4:p.Leu276Pro
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.350T>C
  hgvsp: ENSP00000395885.1:p.Leu117Pro
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.578T>C
  hgvsp: ENSP00000335652.7:p.Leu193Pro
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.827T>C
  hgvsp: ENSP00000384797.3:p.Leu276Pro
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35663
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu276Pro
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

22-30060999-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30060999
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30060999
    reference: chr 22
allele count: 1
allele frequency: 8.625746127039989e-6
allele num: 115932
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.708T>G
  hgvsp: ENSP00000354897.4:p.Asp236Glu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.354T>G
  hgvsp: ENSP00000335160.6:p.Asp118Glu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.831T>G
  hgvsp: ENSP00000384797.3:p.Asp277Glu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.831T>G
  hgvsp: ENSP00000380891.3:p.Asp277Glu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.582T>G
  hgvsp: ENSP00000340626.4:p.Asp194Glu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.831T>G
  hgvsp: ENSP00000344666.4:p.Asp277Glu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.705T>G
  hgvsp: ENSP00000355183.4:p.Asp235Glu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.831T>G
  hgvsp: ENSP00000354529.4:p.Asp277Glu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.582T>G
  hgvsp: ENSP00000335652.7:p.Asp194Glu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.831T>G
  hgvsp: ENSP00000384029.1:p.Asp277Glu
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22725T>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.354T>G
  hgvsp: ENSP00000395885.1:p.Asp118Glu
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7486
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp277Glu
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-30061019-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061019
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061019
    reference: chr 22
allele count: 1
allele frequency: 8.525003836251726e-6
allele num: 117302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.725A>G
  hgvsp: ENSP00000355183.4:p.Lys242Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.851A>G
  hgvsp: ENSP00000380891.3:p.Lys284Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.728A>G
  hgvsp: ENSP00000354897.4:p.Lys243Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.602A>G
  hgvsp: ENSP00000335652.7:p.Lys201Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.851A>G
  hgvsp: ENSP00000384797.3:p.Lys284Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.851A>G
  hgvsp: ENSP00000354529.4:p.Lys284Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.602A>G
  hgvsp: ENSP00000340626.4:p.Lys201Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.851A>G
  hgvsp: ENSP00000384029.1:p.Lys284Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.374A>G
  hgvsp: ENSP00000335160.6:p.Lys125Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.374A>G
  hgvsp: ENSP00000395885.1:p.Lys125Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.851A>G
  hgvsp: ENSP00000344666.4:p.Lys284Arg
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22745A>G
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys284Arg
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

22-30061019-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061019
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061019
    reference: chr 22
allele count: 1
allele frequency: 8.525003836251726e-6
allele num: 117302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.851A>T
  hgvsp: ENSP00000354529.4:p.Lys284Met
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.851A>T
  hgvsp: ENSP00000384797.3:p.Lys284Met
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22745A>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.851A>T
  hgvsp: ENSP00000344666.4:p.Lys284Met
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.851A>T
  hgvsp: ENSP00000380891.3:p.Lys284Met
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.374A>T
  hgvsp: ENSP00000395885.1:p.Lys125Met
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.851A>T
  hgvsp: ENSP00000384029.1:p.Lys284Met
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.725A>T
  hgvsp: ENSP00000355183.4:p.Lys242Met
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.728A>T
  hgvsp: ENSP00000354897.4:p.Lys243Met
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.374A>T
  hgvsp: ENSP00000335160.6:p.Lys125Met
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.602A>T
  hgvsp: ENSP00000340626.4:p.Lys201Met
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.602A>T
  hgvsp: ENSP00000335652.7:p.Lys201Met
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36421
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys284Met
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD

22-30061025-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061025
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061025
    reference: chr 22
allele count: 1
allele frequency: 8.517597356137781e-6
allele num: 117404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.380A>G
  hgvsp: ENSP00000395885.1:p.Asn127Ser
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.857A>G
  hgvsp: ENSP00000354529.4:p.Asn286Ser
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.734A>G
  hgvsp: ENSP00000354897.4:p.Asn245Ser
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.380A>G
  hgvsp: ENSP00000335160.6:p.Asn127Ser
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.857A>G
  hgvsp: ENSP00000380891.3:p.Asn286Ser
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22751A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.608A>G
  hgvsp: ENSP00000340626.4:p.Asn203Ser
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.857A>G
  hgvsp: ENSP00000344666.4:p.Asn286Ser
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.608A>G
  hgvsp: ENSP00000335652.7:p.Asn203Ser
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.731A>G
  hgvsp: ENSP00000355183.4:p.Asn244Ser
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.857A>G
  hgvsp: ENSP00000384029.1:p.Asn286Ser
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.857A>G
  hgvsp: ENSP00000384797.3:p.Asn286Ser
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8372
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn286Ser
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

22-30061035-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061035
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061035
    reference: chr 22
allele count: 1
allele frequency: 8.534025158306167e-6
allele num: 117178
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.867G>A
  hgvsp: ENST00000338641.4:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.390G>A
  hgvsp: ENST00000347330.5:c.390G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.867G>A
  hgvsp: ENST00000361166.4:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.390G>A
  hgvsp: ENST00000432151.1:c.390G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.618G>A
  hgvsp: ENST00000353887.4:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.867G>A
  hgvsp: ENST00000397789.3:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.744G>A
  hgvsp: ENST00000361452.4:c.744G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22761G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.867G>A
  hgvsp: ENST00000403435.1:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.618G>A
  hgvsp: ENST00000334961.7:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.867G>A
  hgvsp: ENST00000403999.3:c.867G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.741G>A
  hgvsp: ENST00000361676.4:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8648
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys289Lys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

22-30061039-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061039
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061039
    reference: chr 22
allele count: 1
allele frequency: 8.551686392556613e-6
allele num: 116936
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.745C>T
  hgvsp: ENSP00000355183.4:p.Arg249Cys
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.871C>T
  hgvsp: ENSP00000384797.3:p.Arg291Cys
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.394C>T
  hgvsp: ENSP00000395885.1:p.Arg132Cys
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.748C>T
  hgvsp: ENSP00000354897.4:p.Arg250Cys
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22765C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.871C>T
  hgvsp: ENSP00000380891.3:p.Arg291Cys
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.622C>T
  hgvsp: ENSP00000335652.7:p.Arg208Cys
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.871C>T
  hgvsp: ENSP00000354529.4:p.Arg291Cys
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.871C>T
  hgvsp: ENSP00000344666.4:p.Arg291Cys
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.871C>T
  hgvsp: ENSP00000384029.1:p.Arg291Cys
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.394C>T
  hgvsp: ENSP00000335160.6:p.Arg132Cys
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.622C>T
  hgvsp: ENSP00000340626.4:p.Arg208Cys
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg291Cys
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

22-30061040-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061040
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061040
    reference: chr 22
allele count: 3
allele frequency: 2.568493150684932e-5
allele num: 116800
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.749G>A
  hgvsp: ENSP00000354897.4:p.Arg250His
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.872G>A
  hgvsp: ENSP00000380891.3:p.Arg291His
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.623G>A
  hgvsp: ENSP00000340626.4:p.Arg208His
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22766G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.746G>A
  hgvsp: ENSP00000355183.4:p.Arg249His
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.395G>A
  hgvsp: ENSP00000335160.6:p.Arg132His
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.872G>A
  hgvsp: ENSP00000384029.1:p.Arg291His
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.623G>A
  hgvsp: ENSP00000335652.7:p.Arg208His
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.395G>A
  hgvsp: ENSP00000395885.1:p.Arg132His
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.872G>A
  hgvsp: ENSP00000354529.4:p.Arg291His
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.872G>A
  hgvsp: ENSP00000384797.3:p.Arg291His
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.872G>A
  hgvsp: ENSP00000344666.4:p.Arg291His
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8741
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34850
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg291His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS

22-30061047-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061047
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061047
    reference: chr 22
allele count: 2
allele frequency: 1.722118895088517e-5
allele num: 116136
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.879T>C
  hgvsp: ENST00000361166.4:c.879T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.879T>C
  hgvsp: ENST00000403435.1:c.879T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.630T>C
  hgvsp: ENST00000334961.7:c.630T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.402T>C
  hgvsp: ENST00000432151.1:c.402T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.756T>C
  hgvsp: ENST00000361452.4:c.756T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.879T>C
  hgvsp: ENST00000397789.3:c.879T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.630T>C
  hgvsp: ENST00000353887.4:c.630T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.879T>C
  hgvsp: ENST00000338641.4:c.879T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22773T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.879T>C
  hgvsp: ENST00000403999.3:c.879T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.753T>C
  hgvsp: ENST00000361676.4:c.753T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.402T>C
  hgvsp: ENST00000347330.5:c.402T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8739
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asn293Asn
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP

22-30061050-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061050
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061050
    reference: chr 22
allele count: 5
allele frequency: 4.310344827586207e-5
allele num: 116000
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.633G>A
  hgvsp: ENST00000353887.4:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.756G>A
  hgvsp: ENST00000361676.4:c.756G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.882G>A
  hgvsp: ENST00000403999.3:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.882G>A
  hgvsp: ENST00000403435.1:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.759G>A
  hgvsp: ENST00000361452.4:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.882G>A
  hgvsp: ENST00000338641.4:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.882G>A
  hgvsp: ENST00000361166.4:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22776G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.882G>A
  hgvsp: ENST00000397789.3:c.882G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.405G>A
  hgvsp: ENST00000347330.5:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.633G>A
  hgvsp: ENST00000334961.7:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.405G>A
  hgvsp: ENST00000432151.1:c.405G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8766
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys294Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/22-30061062-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061062
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061062
    reference: chr 22
allele count: 1
allele frequency: 8.750590664869879e-6
allele num: 114278
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.759+9A>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.885+9A>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22788A>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.762+9A>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.885+9A>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.636+9A>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.885+9A>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.885+9A>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.885+9A>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.408+9A>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.408+9A>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.636+9A>C
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6904
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

22-30061063-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061063
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061063
    reference: chr 22
allele count: 1
allele frequency: 8.762245237719714e-6
allele num: 114126
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.636+10G>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.408+10G>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.885+10G>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.885+10G>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.885+10G>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.759+10G>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.762+10G>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.408+10G>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22789G>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.885+10G>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.885+10G>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.636+10G>C
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8368
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28132
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

22-30061076-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061076
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061076
    reference: chr 22
allele count: 1
allele frequency: 8.948706017109926e-6
allele num: 111748
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.762+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.885+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.636+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.885+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.885+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.408+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.759+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22802A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.885+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.408+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.885+23A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.636+23A>G
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15429
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
reference allele: A
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

22-30061080-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061080
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061080
    reference: chr 22
allele count: 1
allele frequency: 8.984403076259613e-6
allele num: 111304
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.885+27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.408+27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.408+27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.759+27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.762+27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.885+27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.636+27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.885+27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.636+27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.885+27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22806C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.885+27C>T
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16198
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4904
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6238
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

22-30061083-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061083
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061083
    reference: chr 22
allele count: 1
allele frequency: 9.018433678438729e-6
allele num: 110884
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.759+30A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.408+30A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.885+30A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.885+30A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.762+30A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.885+30A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.885+30A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.636+30A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.408+30A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22809A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.885+30A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.636+30A>G
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6441
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

22-30061086-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061086
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061086
    reference: chr 22
allele count: 1
allele frequency: 9.069965715529595e-6
allele num: 110254
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.762+33A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.885+33A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.885+33A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.885+33A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.759+33A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.885+33A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.408+33A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.636+33A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22812A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.885+33A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.636+33A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.408+33A>G
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11133
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8305
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

22-30061088-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061088
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061088
    reference: chr 22
allele count: 4
allele frequency: 3.653168210130235e-5
allele num: 109494
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.885+35G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.636+35G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.759+35G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.636+35G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.762+35G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.885+35G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.885+35G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22814G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.885+35G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.885+35G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.408+35G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.408+35G>A
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9721
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

22-30061095-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061095
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061095
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 104682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.408+42T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.885+42T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.759+42T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.885+42T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.885+42T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.885+42T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.762+42T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22821T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.636+42T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.885+42T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.636+42T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.408+42T>C
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7128
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13264
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

22-30061105-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30061105
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30061105
    reference: chr 22
allele count: 1
allele frequency: 1.003250531722782e-5
allele num: 99676
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.636+52T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.885+52T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.885+52T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.636+52T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.762+52T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.885+52T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.408+52T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.885+52T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+22831T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.408+52T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.885+52T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.759+52T>C
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12727
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

22-30064285-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30064285
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30064285
    reference: chr 22
allele count: 2
allele frequency: 1.78173719376392e-5
allele num: 112250
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.886-37T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.637-37T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.409-37T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.886-37T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.763-37T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+26011T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.886-37T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.637-37T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.886-37T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.760-37T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.409-37T>C
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.886-37T>C
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8395
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21699
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9918
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

22-30064290-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30064290
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30064290
    reference: chr 22
allele count: 26
allele frequency: 2.303902456314465e-4
allele num: 112852
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.886-32A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.886-32A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.409-32A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.637-32A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.763-32A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.886-32A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.760-32A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.637-32A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.886-32A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.886-32A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+26016A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.409-32A>G
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3151
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4008
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24506
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9091
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8088
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

22-30064295-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30064295
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30064295
    reference: chr 22
allele count: 3
allele frequency: 2.635416483651633e-5
allele num: 113834
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.760-27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.886-27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.409-27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.886-27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.763-27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.886-27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.637-27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.637-27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+26021C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.886-27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.409-27C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.886-27C>T
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5763
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9648
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

22-30064300-TTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30064300
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30064298
    reference: chr 22
allele count: 1
allele frequency: 8.667013347200554e-6
allele num: 115380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.886-20_886-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.409-20_409-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.886-20_886-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.886-20_886-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+26028_447+26029delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.637-20_637-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.760-20_760-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.409-20_409-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.637-20_637-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.886-20_886-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.763-20_763-19delGT
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.886-20_886-19delGT
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30564
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: TTG
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum

22-30064302-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30064302
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30064302
    reference: chr 22
allele count: 1
allele frequency: 8.623960812722066e-6
allele num: 115956
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.637-20G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.886-20G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.637-20G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.886-20G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.763-20G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.760-20G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.886-20G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.886-20G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.409-20G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.886-20G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+26028G>A
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.409-20G>A
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10681
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

22-30064307-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30064307
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30064307
    reference: chr 22
allele count: 72
allele frequency: 6.109772241268117e-4
allele num: 117844
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.637-15C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.409-15C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.409-15C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.886-15C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+26033C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.760-15C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.637-15C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.886-15C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.763-15C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.886-15C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.886-15C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.886-15C>T
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11362
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33306
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 3.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ

22-30064327-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30064327
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30064327
    reference: chr 22
allele count: 1
allele frequency: 8.29531314807134e-6
allele num: 120550
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.891C>T
  hgvsp: ENST00000403999.3:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.414C>T
  hgvsp: ENST00000347330.5:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.891C>T
  hgvsp: ENST00000338641.4:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.642C>T
  hgvsp: ENST00000334961.7:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.891C>T
  hgvsp: ENST00000361166.4:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.891C>T
  hgvsp: ENST00000397789.3:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.414C>T
  hgvsp: ENST00000432151.1:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.642C>T
  hgvsp: ENST00000353887.4:c.642C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.768C>T
  hgvsp: ENST00000361452.4:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.765C>T
  hgvsp: ENST00000361676.4:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+26053C>T
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.891C>T
  hgvsp: ENST00000403435.1:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35151
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu297Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

22-30064333-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30064333
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30064333
    reference: chr 22
allele count: 4
allele frequency: 3.31054574346581e-5
allele num: 120826
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.897A>G
  hgvsp: ENST00000338641.4:c.897A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.897A>G
  hgvsp: ENST00000403999.3:c.897A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.897A>G
  hgvsp: ENST00000403435.1:c.897A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.897A>G
  hgvsp: ENST00000397789.3:c.897A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.774A>G
  hgvsp: ENST00000361452.4:c.774A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.771A>G
  hgvsp: ENST00000361676.4:c.771A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.648A>G
  hgvsp: ENST00000334961.7:c.648A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.420A>G
  hgvsp: ENST00000432151.1:c.420A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.420A>G
  hgvsp: ENST00000347330.5:c.420A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.648A>G
  hgvsp: ENST00000353887.4:c.648A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+26059A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.897A>G
  hgvsp: ENST00000361166.4:c.897A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35259
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2631
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu299Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

22-30064337-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30064337
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30064337
    reference: chr 22
allele count: 2
allele frequency: 1.654013463669594e-5
allele num: 120918
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.424A>G
  hgvsp: ENSP00000335160.6:p.Ile142Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.901A>G
  hgvsp: ENSP00000344666.4:p.Ile301Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.901A>G
  hgvsp: ENSP00000354529.4:p.Ile301Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.901A>G
  hgvsp: ENSP00000380891.3:p.Ile301Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.652A>G
  hgvsp: ENSP00000335652.7:p.Ile218Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.424A>G
  hgvsp: ENSP00000395885.1:p.Ile142Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.901A>G
  hgvsp: ENSP00000384797.3:p.Ile301Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.775A>G
  hgvsp: ENSP00000355183.4:p.Ile259Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+26063A>G
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.901A>G
  hgvsp: ENSP00000384029.1:p.Ile301Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.652A>G
  hgvsp: ENSP00000340626.4:p.Ile218Val
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.778A>G
  hgvsp: ENSP00000354897.4:p.Ile260Val
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12661
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile301Val
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

22-30064339-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 30064339
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 30064339
    reference: chr 22
allele count: 1
allele frequency: 8.267879288962381e-6
allele num: 120950
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354897
  ensembl transcript: ENST00000361452
  gene symbol: NF2
  hgvsc: ENST00000361452.4:c.780C>T
  hgvsp: ENST00000361452.4:c.780C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000354529
  ensembl transcript: ENST00000361166
  gene symbol: NF2
  hgvsc: ENST00000361166.4:c.903C>T
  hgvsp: ENST00000361166.4:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000340626
  ensembl transcript: ENST00000353887
  gene symbol: NF2
  hgvsc: ENST00000353887.4:c.654C>T
  hgvsp: ENST00000353887.4:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384029
  ensembl transcript: ENST00000403435
  gene symbol: NF2
  hgvsc: ENST00000403435.1:c.903C>T
  hgvsp: ENST00000403435.1:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000384797
  ensembl transcript: ENST00000403999
  gene symbol: NF2
  hgvsc: ENST00000403999.3:c.903C>T
  hgvsp: ENST00000403999.3:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000344666
  ensembl transcript: ENST00000338641
  gene symbol: NF2
  hgvsc: ENST00000338641.4:c.903C>T
  hgvsp: ENST00000338641.4:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000395885
  ensembl transcript: ENST00000432151
  gene symbol: NF2
  hgvsc: ENST00000432151.1:c.426C>T
  hgvsp: ENST00000432151.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000380891
  ensembl transcript: ENST00000397789
  gene symbol: NF2
  hgvsc: ENST00000397789.3:c.903C>T
  hgvsp: ENST00000397789.3:c.903C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000355183
  ensembl transcript: ENST00000361676
  gene symbol: NF2
  hgvsc: ENST00000361676.4:c.777C>T
  hgvsp: ENST00000361676.4:c.777C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335160
  ensembl transcript: ENST00000347330
  gene symbol: NF2
  hgvsc: ENST00000347330.5:c.426C>T
  hgvsp: ENST00000347330.5:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000335652
  ensembl transcript: ENST00000334961
  gene symbol: NF2
  hgvsc: ENST00000334961.7:c.654C>T
  hgvsp: ENST00000334961.7:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7773
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000186575
  ensembl protein: ENSP00000409921
  ensembl transcript: ENST00000413209
  gene symbol: NF2
  hgvsc: ENST00000413209.2:c.447+26065C>T
  variant of: http://identifiers.org/hgnc/7773
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12696
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile301Ile
num of homozygotes: 0
reference allele: C

GenotypeDepth
all individuals: 9338
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 825
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53213
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 72
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2351
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.24e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.454e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.925e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.177e1

DP
type: SiteQuality
SIO_000300: 4.246658e6

VQSLOD
type: SiteQuality
SIO_000300: -2.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.899e1

GenotypeDepth
all individuals: 5272
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 828
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1023
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2338
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 916
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53214
bin: 9.75e1
variant carriers: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.693679720822024e-5
allele num: 10316
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

FS
type: SiteQuality
SIO_000300: 1.737e0

MQRankSum
type: SiteQuality
SIO_000300: -1.88e-1

DP
type: SiteQuality
SIO_000300: 4.246895e6

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 1.256e1

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.88e-1

GenotypeDepth
all individuals: 5013
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 938
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53214
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 85
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2490
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 851
bin: 8.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.897430944562488e-4
allele num: 10354
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

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

DP
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SIO_000300: 4.24839e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.83e0

QD
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SIO_000300: 1.031e1

MQRankSum
type: SiteQuality
SIO_000300: 9.53e-1

FS
type: SiteQuality
SIO_000300: 3.273e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.41e0

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
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
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997691777331455e-5
allele num: 66718
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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.48e-1

MQRankSum
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SIO_000300: 7.25e-1

BaseQRankSum
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FS
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VQSLOD
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ReadPosRankSum
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DP
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MQ
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SIO_000300: 5.953e1

QD
type: SiteQuality
SIO_000300: 1.182e1

InbreedingCoeff
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SIO_000300: -1.0e-4

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.75e-1

ReadPosRankSum
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MQ
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SIO_000300: 5.952e1

DP
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InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
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SIO_000300: -1.599e0

QD
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SIO_000300: 1.401e1

FS
type: SiteQuality
SIO_000300: 1.858e0

MQRankSum
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SIO_000300: -2.93e-1

ClippingRankSum
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SIO_000300: 3.05e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -2.91e-1

VQSLOD
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ClippingRankSum
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FS
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InbreedingCoeff
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MQ
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BaseQRankSum
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ReadPosRankSum
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DP
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SIO_000300: 4.2505e6

QD
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SIO_000300: 1.316e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

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

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

Other
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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

African
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allele frequency: 1.923816852635629e-4
allele num: 10396
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

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

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

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66736
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South Asian
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Latino
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allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

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

Other
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Latino
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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ReadPosRankSum
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InbreedingCoeff
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QD
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VQSLOD
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ClippingRankSum
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FS
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MQ
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BaseQRankSum
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MQRankSum
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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Other
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 9.617234083477592e-5
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European (Non-Finnish)
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ClippingRankSum
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DP
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VQSLOD
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FS
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MQRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

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

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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African
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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East Asian
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European (Non-Finnish)
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allele num: 66718
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African
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Other
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South Asian
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DP
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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QD
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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FS
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MQ
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Finnish)
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European (Non-Finnish)
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Other
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East Asian
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Latino
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MQRankSum
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VQSLOD
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DP
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BaseQRankSum
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FS
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ReadPosRankSum
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MQ
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QD
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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East Asian
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FS
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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InbreedingCoeff
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

GenotypeQuality
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GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8640
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 8.997390756680563e-5
allele num: 66686
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.593809441466367e-4
allele num: 11566
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 4.24813e6

VQSLOD
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SIO_000300: 7.89e-1

MQRankSum
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SIO_000300: -4.0e-1

QD
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ReadPosRankSum
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SIO_000300: 2.3e-1

BaseQRankSum
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SIO_000300: -3.187e0

ClippingRankSum
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SIO_000300: -5.04e-1

FS
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 908
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.928268414963363e-4
allele num: 10372
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 6.66e-1

MQ
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SIO_000300: 5.979e1

MQRankSum
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SIO_000300: -8.04e-1

BaseQRankSum
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InbreedingCoeff
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DP
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QD
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ReadPosRankSum
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SIO_000300: 2.93e-1

FS
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SIO_000300: 3.319e0

ClippingRankSum
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SIO_000300: 3.05e-1

GenotypeDepth
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variant carriers: 1

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 1
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allele num: 66546
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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DP
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SIO_000300: 4.242656e6

BaseQRankSum
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MQ
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QD
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VQSLOD
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InbreedingCoeff
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SIO_000300: -1.0e-4

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 4.38e-1

MQRankSum
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SIO_000300: 2.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 2

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

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

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

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.50815976918222e-5
allele num: 66546
num of homozygotes: 0

MQ
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SIO_000300: 5.966e1

ReadPosRankSum
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SIO_000300: 3.42e-1

FS
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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SIO_000300: 4.242592e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.22e-1

QD
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SIO_000300: 1.495e1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

African
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allele frequency: 3.866228494104001e-4
allele num: 10346
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East Asian
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Other
type: Population
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Latino
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European (Non-Finnish)
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allele num: 66488
num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66488
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Other
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African
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European (Finnish)
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allele num: 6602
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Latino
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66482
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.665571235260003e-5
allele num: 10346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.92e-1

InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
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SIO_000300: -1.323e0

FS
type: SiteQuality
SIO_000300: 4.076e0

MQRankSum
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SIO_000300: 3.8e-2

BaseQRankSum
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SIO_000300: 1.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.89e-1

DP
type: SiteQuality
SIO_000300: 4.238906e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.107e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 9

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

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.027000964320154e-5
allele num: 66368
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 3.472825143254037e-4
allele num: 11518
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-2

FS
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QD
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VQSLOD
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ReadPosRankSum
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DP
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SIO_000300: 4.234686e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.5e-2

BaseQRankSum
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SIO_000300: -3.232e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.683570684265369e-5
allele num: 11516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8528
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.710623422023694e-5
allele num: 10298
num of homozygotes: 0

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

InbreedingCoeff
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SIO_000300: 5.7e-3

MQRankSum
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ReadPosRankSum
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FS
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DP
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ClippingRankSum
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SIO_000300: 1.36e-1

VQSLOD
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SIO_000300: 4.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.857e0

QD
type: SiteQuality
SIO_000300: 1.081e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 195
bin: 4.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.708737864077671e-5
allele num: 10300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66332
num of homozygotes: 0

Other
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ClippingRankSum
type: SiteQuality
SIO_000300: 9.429999999999999e-1

FS
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SIO_000300: 1.531e1

BaseQRankSum
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SIO_000300: -4.88e0

MQRankSum
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VQSLOD
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SIO_000300: -2.101e0

InbreedingCoeff
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SIO_000300: 6.2e-3

MQ
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SIO_000300: 5.882e1

QD
type: SiteQuality
SIO_000300: 1.585e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-2

DP
type: SiteQuality
SIO_000300: 4.234219e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7016
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.059155724975294e-5
allele num: 14166
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 52622
num of homozygotes: 0

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

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

Other
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ClippingRankSum
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SIO_000300: -1.425e0

BaseQRankSum
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QD
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MQ
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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SIO_000300: 7.98e-1

FS
type: SiteQuality
SIO_000300: 1.944e0

DP
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 52482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7012
num of homozygotes: 0

African
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allele frequency: 1.088613106901807e-4
allele num: 9186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8906
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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ClippingRankSum
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QD
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MQRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 1.057e0

DP
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SIO_000300: 1.530113e6

MQ
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SIO_000300: 6.081e1

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 1
allele frequency: 7.010656197420079e-5
allele num: 14264
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 9044
num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7547
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9252
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 4.794134235758601e-3
allele num: 7092
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: 1.402131239484016e-4
allele num: 14264
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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QD
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FS
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 0

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

African
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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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.849522823111637e-5
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

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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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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.818446319464649e-5
allele num: 54992
num of homozygotes: 0

DP
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MQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQ
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QD
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BaseQRankSum
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SIO_000300: 3.28e0

VQSLOD
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ClippingRankSum
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SIO_000300: -9.5e-2

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9446
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.891798759476223e-5
allele num: 14510
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 55090
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7392
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: 1.51e0

MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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FS
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MQ
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SIO_000300: 5.998e1

ClippingRankSum
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SIO_000300: 1.4e-2

DP
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SIO_000300: 1.661473e6

ReadPosRankSum
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SIO_000300: 1.65e-1

GenotypeDepth
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 24

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 812
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 2.303182579564489e-3
allele num: 9552
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: 2.044571662236761e-4
allele num: 9782
num of homozygotes: 0

South Asian
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East Asian
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QD
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MQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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BaseQRankSum
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DP
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InbreedingCoeff
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SIO_000300: -1.5e-3

ClippingRankSum
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MQ
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GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7784
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6100
num of homozygotes: 0

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

Other
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allele count: 1
allele frequency: 1.219512195121951e-3
allele num: 820
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 824
num of homozygotes: 0

Latino
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allele frequency: 9.777082518576456e-5
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num of homozygotes: 0

East Asian
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South Asian
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European (Finnish)
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European (Non-Finnish)
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African
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MQRankSum
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BaseQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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FS
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VQSLOD
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62760
num of homozygotes: 0

South Asian
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allele frequency: 1.283697047496791e-4
allele num: 15580
num of homozygotes: 0

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

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

African
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South Asian
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East Asian
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European (Non-Finnish)
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Latino
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num of homozygotes: 0

European (Finnish)
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DP
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FS
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InbreedingCoeff
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QD
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MQRankSum
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MQ
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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European (Finnish)
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European (Non-Finnish)
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East Asian
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South Asian
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QD
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MQ
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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FS
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ClippingRankSum
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InbreedingCoeff
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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East Asian
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Other
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African
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Latino
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South Asian
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MQ
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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DP
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InbreedingCoeff
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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South Asian
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Other
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InbreedingCoeff
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QD
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VQSLOD
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ReadPosRankSum
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FS
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BaseQRankSum
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MQRankSum
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MQ
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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East Asian
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South Asian
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African
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Latino
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ReadPosRankSum
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QD
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FS
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 307
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10138
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564064064064064e-5
allele num: 63936
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15814
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11212
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

DP
type: SiteQuality
SIO_000300: 1.900857e6

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.73e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.791e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

QD
type: SiteQuality
SIO_000300: 1.185e1

GenotypeDepth
all individuals: 537
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 418
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GenotypeDepth
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GenotypeQuality
all individuals: 614
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9685
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variant carriers: 3

GenotypeQuality
all individuals: 503
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.785714285714286e-4
allele num: 11200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.566023552994237e-5
allele num: 63856
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: 8454
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.638e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.36e-1

DP
type: SiteQuality
SIO_000300: 1.898678e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.92e1

QD
type: SiteQuality
SIO_000300: 1.054e1

FS
type: SiteQuality
SIO_000300: 1.7372e1

GenotypeDepth
all individuals: 536
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variant carriers: 0

GenotypeDepth
all individuals: 711
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variant carriers: 0

GenotypeDepth
all individuals: 2250
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.906875371507826e-5
allele num: 10094
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.971828458639871e-5
allele num: 11146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63416
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15722
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.28e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.879999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 1.405e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.54e-1

DP
type: SiteQuality
SIO_000300: 1.883177e6

GenotypeDepth
all individuals: 813
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 730
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 761
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 539
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variant carriers: 0

GenotypeQuality
all individuals: 224
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variant carriers: 0

GenotypeQuality
all individuals: 593
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GenotypeQuality
all individuals: 216
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GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 715
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variant carriers: 0

GenotypeQuality
all individuals: 355
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 557
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GenotypeQuality
all individuals: 6
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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: 9687
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variant carriers: 5

GenotypeQuality
all individuals: 38872
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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
all individuals: 276
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variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63310
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10076
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15718
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 5.946717411988582e-4
allele num: 8408
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

FS
type: SiteQuality
SIO_000300: 6.12e-1

QD
type: SiteQuality
SIO_000300: 8.130000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.651e0

DP
type: SiteQuality
SIO_000300: 1.881016e6

GenotypeDepth
all individuals: 671
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9681
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2256
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variant carriers: 0

GenotypeQuality
all individuals: 1374
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variant carriers: 0

GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 629
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 164
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 7960
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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
all individuals: 324
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variant carriers: 0

GenotypeQuality
all individuals: 331
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variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62212
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6410
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8286
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.441638752898738e-5
allele num: 15524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10938
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10042
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.94e-1

BaseQRankSum
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SIO_000300: -3.694e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.8e-1

QD
type: SiteQuality
SIO_000300: 1.073e1

MQ
type: SiteQuality
SIO_000300: 5.979e1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 1.981e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

DP
type: SiteQuality
SIO_000300: 1.828285e6

VQSLOD
type: SiteQuality
SIO_000300: 6.52e-1

GenotypeDepth
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variant carriers: 0

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

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

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 2238
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10038
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.610357821507939e-5
allele num: 62098
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6410
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15518
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10926
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.575e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

DP
type: SiteQuality
SIO_000300: 1.822219e6

MQ
type: SiteQuality
SIO_000300: 5.91e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.542e0

FS
type: SiteQuality
SIO_000300: 8.403e0

ReadPosRankSum
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SIO_000300: 1.65e0

VQSLOD
type: SiteQuality
SIO_000300: -7.179e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 493
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GenotypeQuality
all individuals: 1744
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.43040362127499e-5
allele num: 10604
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60650
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9904
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.053e1

DP
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MQ
type: SiteQuality
SIO_000300: 5.893e1

MQRankSum
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BaseQRankSum
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SIO_000300: 4.95e-1

ClippingRankSum
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ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 9.704000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
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SIO_000300: -1.569e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9683
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

Other
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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

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

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

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
allele num: 15282
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.656067832538421e-5
allele num: 60384
num of homozygotes: 0

BaseQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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MQ
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MQRankSum
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QD
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SIO_000300: 8.77e0

DP
type: SiteQuality
SIO_000300: 1.683095e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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East Asian
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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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European (Non-Finnish)
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allele count: 1
allele frequency: 1.664225802156837e-5
allele num: 60088
num of homozygotes: 0

Other
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DP
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BaseQRankSum
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ReadPosRankSum
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QD
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MQ
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MQRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: -8.0e-4

FS
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.675434775324197e-5
allele num: 59686
num of homozygotes: 0

Latino
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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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
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SIO_000300: 1.625388e6

ReadPosRankSum
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QD
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MQ
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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VQSLOD
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FS
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BaseQRankSum
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SIO_000300: 3.95e0

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 15132
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7920
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6250
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
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.75995403231258e-5
allele num: 59172
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e-1

DP
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SIO_000300: 1.610359e6

FS
type: SiteQuality
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InbreedingCoeff
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QD
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VQSLOD
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BaseQRankSum
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SIO_000300: -1.791e0

MQ
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SIO_000300: 5.966e1

MQRankSum
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SIO_000300: 3.9e-2

ReadPosRankSum
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SIO_000300: 6.21e-1

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7564
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6096
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 56152
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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

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

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

Other
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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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African
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allele frequency: 1.071122536418166e-4
allele num: 9336
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: 1.74e-1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 718
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Latino
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allele frequency: 0.0e0
allele num: 10644
num of homozygotes: 0

East Asian
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African
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allele frequency: 2.107037505267594e-4
allele num: 9492
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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Other
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MQRankSum
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ClippingRankSum
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FS
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DP
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele num: 860
num of homozygotes: 0

African
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allele frequency: 2.302700439606448e-3
allele num: 9554
num of homozygotes: 0

East Asian
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European (Non-Finnish)
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allele frequency: 4.798925040790863e-5
allele num: 62514
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European (Finnish)
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.533e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

VQSLOD
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MQ
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SIO_000300: 6.0e1

ReadPosRankSum
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SIO_000300: 2.14e-1

FS
type: SiteQuality
SIO_000300: 7.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.15e-1

DP
type: SiteQuality
SIO_000300: 1.827581e6

BaseQRankSum
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SIO_000300: 3.24e0

GenotypeDepth
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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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
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63114
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6150
num of homozygotes: 0

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

Latino
type: Population
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

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: 3
allele frequency: 1.955416503715291e-4
allele num: 15342
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.866e1

FS
type: SiteQuality
SIO_000300: 3.522e0

DP
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ClippingRankSum
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SIO_000300: 1.39e-1

QD
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ReadPosRankSum
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SIO_000300: -1.01e-1

InbreedingCoeff
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SIO_000300: -1.5e-3

BaseQRankSum
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SIO_000300: -2.627e0

MQRankSum
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SIO_000300: 1.01e-1

VQSLOD
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SIO_000300: -1.194e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10980
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9814
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6214
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64002
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.2453300124533e-4
allele num: 8030
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.81e0

QD
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SIO_000300: 2.909e1

InbreedingCoeff
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SIO_000300: -9.0e-4

DP
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SIO_000300: 1.905835e6

ClippingRankSum
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SIO_000300: 2.28e-1

ReadPosRankSum
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SIO_000300: -5.01e-1

FS
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.102e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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
all individuals: 38263
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variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.051412020275162e-5
allele num: 11048
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64314
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9874
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8092
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15528
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.04e-1

DP
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SIO_000300: 1.920884e6

FS
type: SiteQuality
SIO_000300: 2.658e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.386e0

VQSLOD
type: SiteQuality
SIO_000300: -2.604e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

QD
type: SiteQuality
SIO_000300: 7.11e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9096
bin: 9.75e1
variant carriers: 71

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8312
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.780626780626781e-4
allele num: 11232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 67
allele frequency: 1.026851397743992e-3
allele num: 65248
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.979805979014057e-4
allele num: 10102
num of homozygotes: 0

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

European (Finnish)
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allele count: 1
allele frequency: 1.58378207158695e-4
allele num: 6314
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15754
num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 7.900000000000001e-3

VQSLOD
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ReadPosRankSum
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DP
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ClippingRankSum
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QD
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MQRankSum
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SIO_000300: 1.6e-2

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -2.793e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 778
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505072092953252e-5
allele num: 66442
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 896
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

MQ
type: SiteQuality
SIO_000300: 5.895e1

InbreedingCoeff
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ReadPosRankSum
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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SIO_000300: 1.995465e6

QD
type: SiteQuality
SIO_000300: 3.75e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66528
num of homozygotes: 0

African
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South Asian
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allele count: 4
allele frequency: 2.445585717779408e-4
allele num: 16356
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6536
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VQSLOD
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SIO_000300: 1.12e0

InbreedingCoeff
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BaseQRankSum
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DP
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ReadPosRankSum
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FS
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ClippingRankSum
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MQRankSum
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MQ
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QD
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SIO_000300: 1.356e1

GenotypeDepth
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

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

East Asian
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
allele num: 10382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004807692307692e-5
allele num: 66560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.924e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.23e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.79e-1

FS
type: SiteQuality
SIO_000300: 2.984e0

DP
type: SiteQuality
SIO_000300: 2.001349e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.17e-1

QD
type: SiteQuality
SIO_000300: 1.309e1

GenotypeDepth
all individuals: 642
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 601
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 496
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 405
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3952
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44810
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0