22-45255721-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255721
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255721
    reference: chr 22
allele count: 1
allele frequency: 8.429428821903027e-6
allele num: 118632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+7G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+7G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+7G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+7G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+7G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+7G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+7G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2434G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+7G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+7G>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2365
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2451
  bin: 7.75e1
  variant carriers: 0
hgvs: c.1347+7G>A
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

22-45255722-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255722
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255722
    reference: chr 22
allele count: 16
allele frequency: 1.348617666891436e-4
allele num: 118640
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+8G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+8G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+8G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+8G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+8G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+8G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+8G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+8G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2433G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+8G>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23495
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7101
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16210
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1491
  bin: 5.25e1
  variant carriers: 0
hgvs: c.1347+8G>A
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

22-45255724-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255724
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255724
    reference: chr 22
allele count: 1
allele frequency: 8.437394532568342e-6
allele num: 118520
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+10G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+10G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+10G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+10G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2431G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+10G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+10G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+10G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+10G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+10G>C
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2376
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2067
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2454
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3737
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

22-45255726-A-AGGGGGGAGCTTG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255726
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255738
    reference: chr 22
allele count: 1
allele frequency: 8.447372867038351e-6
allele num: 118380
alternate allele: AGGGGGGAGCTTG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 6989
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1283
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30964
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2463
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1236
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

22-45255726-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255726
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255725
    reference: chr 22
allele count: 1
allele frequency: 8.447372867038351e-6
allele num: 118380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+18delG
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+18delG
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+18delG
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+18delG
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2423delG
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+18delG
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+18delG
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+18delG
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+18delG
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+18delG
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16109
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6989
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1612
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6400
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: AG
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum

22-45255727-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255727
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255727
    reference: chr 22
allele count: 1
allele frequency: 8.501666326600013e-6
allele num: 117624
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+13G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+13G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+13G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+13G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+13G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2428G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+13G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+13G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+13G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+13G>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14126
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 882
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

22-45255727-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255727
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255727
    reference: chr 22
allele count: 27534
allele frequency: 2.340848806366048e-1
allele num: 117624
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+13G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+13G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+13G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2428G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+13G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+13G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+13G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+13G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+13G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+13G>C
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 3.75e1
  variant carriers: 3338
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 226
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 456
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.25e1
  variant carriers: 337
genotype depth: GenotypeDepth
  all individuals: 14126
  bin: 2.25e1
  variant carriers: 2565
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 14463
  bin: 2.75e1
  variant carriers: 3673
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 4.75e1
  variant carriers: 1813
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.25e1
  variant carriers: 202
genotype depth: GenotypeDepth
  all individuals: 7963
  bin: 3.25e1
  variant carriers: 3876
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 1.25e1
  variant carriers: 339
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.5e0
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 141
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 6.25e1
  variant carriers: 683
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.75e1
  variant carriers: 283
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 5.25e1
  variant carriers: 1374
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.75e1
  variant carriers: 958
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 4.25e1
  variant carriers: 2570
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 1.75e1
  variant carriers: 1167
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 4.75e1
  variant carriers: 90
genotype quality: GenotypeQuality
  all individuals: 882
  bin: 3.75e1
  variant carriers: 79
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 7.5e0
  variant carriers: 26
num of homozygotes: 3533
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

22-45255727-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255727
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255727
    reference: chr 22
allele count: 1
allele frequency: 8.501666326600013e-6
allele num: 117624
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+13G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+13G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+13G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+13G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+13G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+13G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2428G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+13G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+13G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+13G>T
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4739
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14463
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1459
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23355
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

22-45255728-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255728
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255728
    reference: chr 22
allele count: 1
allele frequency: 8.587966541282354e-6
allele num: 116442
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+14G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+14G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+14G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+14G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+14G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+14G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2427G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+14G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+14G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+14G>A
  variant of: http://identifiers.org/hgnc/34512
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3839
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9065
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7051
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28192
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

22-45255728-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255728
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255728
    reference: chr 22
allele count: 90
allele frequency: 7.72916988715412e-4
allele num: 116442
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+14G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+14G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+14G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+14G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2427G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+14G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+14G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+14G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+14G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+14G>C
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7373
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14317
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 18728
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3839
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9065
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1071
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

22-45255728-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255728
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255728
    reference: chr 22
allele count: 16
allele frequency: 1.374074646605177e-4
allele num: 116442
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+14G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+14G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2427G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+14G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+14G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+14G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+14G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+14G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+14G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+14G>T
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3839
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9065
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18728
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14317
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7373
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1071
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2353
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

22-45255730-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255730
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255730
    reference: chr 22
allele count: 4
allele frequency: 3.4349506225848e-5
allele num: 116450
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+16G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2425G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+16G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+16G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+16G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+16G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+16G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+16G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+16G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+16G>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7071
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18752
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3797
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14642
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9112
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2344
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

22-45255732-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255732
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255732
    reference: chr 22
allele count: 274
allele frequency: 2.352941176470588e-3
allele num: 116450
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+18G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+18G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+18G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+18G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+18G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+18G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+18G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+18G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2423G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+18G>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18777
  bin: 2.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 6889
  bin: 3.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.25e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9170
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 3.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 14819
  bin: 2.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5611
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

22-45255732-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255732
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255732
    reference: chr 22
allele count: 1
allele frequency: 8.587376556462001e-6
allele num: 116450
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2423G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+18G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+18G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+18G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+18G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+18G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+18G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+18G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+18G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+18G>C
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9170
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5611
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3163
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

22-45255732-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255732
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255733
    reference: chr 22
allele count: 229
allele frequency: 1.966509231429798e-3
allele num: 116450
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+19dupA
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+19dupA
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+19dupA
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+19dupA
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2422dupA
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+19dupA
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+19dupA
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+19dupA
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+19dupA
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+19dupA
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 1.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18777
  bin: 2.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 3.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 9170
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 14819
  bin: 2.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 6889
  bin: 3.25e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 3
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

22-45255735-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255735
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255735
    reference: chr 22
allele count: 7
allele frequency: 6.03448275862069e-5
allele num: 116000
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+21C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2420C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+21C>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+21C>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+21C>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+21C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+21C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+21C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+21C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+21C>G
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14254
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

22-45255735-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255735
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255735
    reference: chr 22
allele count: 4
allele frequency: 3.448275862068966e-5
allele num: 116000
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+21C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+21C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+21C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+21C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+21C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+21C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+21C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2420C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+21C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+21C>T
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4688
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14254
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6471
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2041
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 554
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2763
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5450
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

22-45255738-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255738
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255738
    reference: chr 22
allele count: 1
allele frequency: 8.64274355251331e-6
allele num: 115704
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+24G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+24G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+24G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+24G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+24G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2417G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+24G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+24G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+24G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+24G>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6076
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11734
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13386
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8580
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

22-45255741-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255741
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255741
    reference: chr 22
allele count: 2
allele frequency: 1.739251426186169e-5
allele num: 114992
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+27G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+27G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+27G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+27G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+27G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+27G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+27G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+27G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+27G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2414G>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10073
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12982
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1063
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

22-45255743-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255743
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255743
    reference: chr 22
allele count: 1
allele frequency: 8.70852564660803e-6
allele num: 114830
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+29G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2412G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+29G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+29G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+29G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+29G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+29G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+29G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+29G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+29G>A
  variant of: http://identifiers.org/hgnc/34512
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2795
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12920
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10035
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4244
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9479
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20706
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

22-45255747-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255747
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255747
    reference: chr 22
allele count: 3
allele frequency: 2.628351147713334e-5
allele num: 114140
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+33C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2408C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+33C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+33C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+33C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+33C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+33C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+33C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+33C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+33C>T
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13681
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11662
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11203
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

22-45255748-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255748
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255748
    reference: chr 22
allele count: 1
allele frequency: 8.758868354208636e-6
allele num: 114170
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+34C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+34C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+34C>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+34C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+34C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+34C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+34C>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+34C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+34C>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2407C>G
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4541
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9765
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

22-45255748-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255748
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255748
    reference: chr 22
allele count: 1
allele frequency: 8.758868354208636e-6
allele num: 114170
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+34C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+34C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2407C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+34C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+34C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+34C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+34C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+34C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+34C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+34C>T
  variant of: http://identifiers.org/hgnc/34512
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11032
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13762
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11111
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18104
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1567
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

22-45255749-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255749
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255749
    reference: chr 22
allele count: 157
allele frequency: 1.380511052881487e-3
allele num: 113726
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+35C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+35C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+35C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+35C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+35C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2406C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+35C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+35C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+35C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+35C>T
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13488
  bin: 1.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3152
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13752
  bin: 1.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 10345
  bin: 2.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1861
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 10745
  bin: 2.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9653
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5526
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/22-45255750-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255750
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255750
    reference: chr 22
allele count: 1
allele frequency: 8.785647765809773e-6
allele num: 113822
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+36A>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+36A>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+36A>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+36A>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2405A>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+36A>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+36A>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+36A>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+36A>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+36A>C
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10825
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13427
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13815
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1540
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-45255751-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255751
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255751
    reference: chr 22
allele count: 1
allele frequency: 8.78981787497363e-6
allele num: 113768
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+37G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+37G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+37G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+37G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2404G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+37G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+37G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+37G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+37G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+37G>T
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13871
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13799
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1850
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

22-45255752-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255752
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255752
    reference: chr 22
allele count: 1
allele frequency: 8.818031110013756e-6
allele num: 113404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+38T>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+38T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+38T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2403T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+38T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+38T>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+38T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+38T>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+38T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+38T>G
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14667
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13741
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1844
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2324
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7239
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD

22-45255753-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255753
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255753
    reference: chr 22
allele count: 2
allele frequency: 1.76541204717181e-5
allele num: 113288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+39G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2402G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+39G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+39G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+39G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+39G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+39G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+39G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+39G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+39G>A
  variant of: http://identifiers.org/hgnc/34512
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14638
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13747
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15354
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7214
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

22-45255754-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255754
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255754
    reference: chr 22
allele count: 1
allele frequency: 8.850340738118417e-6
allele num: 112990
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+40G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+40G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+40G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+40G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2401G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+40G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+40G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+40G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+40G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+40G>C
  variant of: http://identifiers.org/hgnc/34512
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14994
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13715
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10760
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3403
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6173
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14745
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

22-45255757-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255757
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255757
    reference: chr 22
allele count: 1
allele frequency: 8.913450396648543e-6
allele num: 112190
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+43T>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+43T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+43T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+43T>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+43T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+43T>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2398T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+43T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+43T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+43T>C
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15341
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13562
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1043
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP

22-45255761-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255761
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255761
    reference: chr 22
allele count: 1
allele frequency: 9.002358617957905e-6
allele num: 111082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+47C>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2394C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+47C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+47C>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+47C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+47C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+47C>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+47C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+47C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+47C>G
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6937
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15156
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1243
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4454
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum

22-45255762-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255762
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255762
    reference: chr 22
allele count: 1
allele frequency: 9.017620430320846e-6
allele num: 110894
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+48T>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2393T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+48T>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+48T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+48T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+48T>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+48T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+48T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+48T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+48T>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6825
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13395
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1466
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9283
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7616
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

22-45255763-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255763
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255763
    reference: chr 22
allele count: 36
allele frequency: 3.261696807161237e-4
allele num: 110372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+49C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+49C>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+49C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+49C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+49C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+49C>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+49C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+49C>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2392C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+49C>G
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13348
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12903
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4326
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6738
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15079
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7651
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1460
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/22-45255764-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255764
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255764
    reference: chr 22
allele count: 6
allele frequency: 5.5005500550055e-5
allele num: 109080
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+50C>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+50C>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+50C>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+50C>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+50C>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+50C>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+50C>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+50C>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+50C>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2391C>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6854
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12880
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13273
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15047
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6983
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4511
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7409
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

22-45255764-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255764
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255764
    reference: chr 22
allele count: 3
allele frequency: 2.75027502750275e-5
allele num: 109080
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2391C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+50C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+50C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+50C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+50C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+50C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+50C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+50C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+50C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+50C>T
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6854
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13273
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1804
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15047
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7656
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1078
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

22-45255765-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255765
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255765
    reference: chr 22
allele count: 2
allele frequency: 1.831870889739691e-5
allele num: 109178
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+51C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+51C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+51C>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+51C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+51C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+51C>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+51C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+51C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2390C>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+51C>G
  variant of: http://identifiers.org/hgnc/34512
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15025
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12845
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6881
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7670
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3285
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2536
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

22-45255765-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255765
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255765
    reference: chr 22
allele count: 2
allele frequency: 1.831870889739691e-5
allele num: 109178
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2390C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+51C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+51C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+51C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+51C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+51C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+51C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+51C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+51C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+51C>T
  variant of: http://identifiers.org/hgnc/34512
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15025
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13300
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4516
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3285
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2536
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/22-45255766-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255766
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255766
    reference: chr 22
allele count: 2
allele frequency: 1.824218322448831e-5
allele num: 109636
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+52A>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+52A>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+52A>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+52A>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+52A>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+52A>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2389A>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+52A>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+52A>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+52A>C
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15001
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13332
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2401
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4527
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5103
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

22-45255766-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45255766
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45255766
    reference: chr 22
allele count: 1
allele frequency: 9.121091612244154e-6
allele num: 109636
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1193+52A>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1074+52A>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.174+52A>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1374+52A>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-2389A>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1347+52A>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*806+52A>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.981+52A>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1611+52A>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1611+52A>G
  variant of: http://identifiers.org/hgnc/34512
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6915
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15001
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4423
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7707
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1043
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

22-45258105-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258105
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258105
    reference: chr 22
allele count: 1
allele frequency: 9.11726627887894e-6
allele num: 109682
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-50C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-50C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-50C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-50C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-50C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-50C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-50C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-50C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-50C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-50C>T
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12168
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7744
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum

22-45258106-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258106
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258106
    reference: chr 22
allele count: 255
allele frequency: 2.326048089904039e-3
allele num: 109628
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-49C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-49C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-49C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-49C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-49C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-49C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-49C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-49C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-49C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-49C>T
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 7760
  bin: 3.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12201
  bin: 2.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 8183
  bin: 2.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11218
  bin: 3.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 5.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 1.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 3288
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6039
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-45258107-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258107
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258107
    reference: chr 22
allele count: 10
allele frequency: 9.113111945467138e-5
allele num: 109732
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-48G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-48G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-48G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-48G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-48G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-48G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-48G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-48G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-48G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-48G>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7797
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12252
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3322
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4113
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 586
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD

22-45258107-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258107
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258107
    reference: chr 22
allele count: 2
allele frequency: 1.822622389093428e-5
allele num: 109732
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-48G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-48G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-48G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-48G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-48G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-48G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-48G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-48G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-48G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-48G>C
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7797
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12252
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1344
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4768
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3322
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

22-45258107-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258107
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258107
    reference: chr 22
allele count: 8
allele frequency: 7.290489556373711e-5
allele num: 109732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-48G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-48G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-48G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-48G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-48G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-48G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-48G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-48G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-48G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-48G>T
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7797
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11350
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12252
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

22-45258108-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258108
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258108
    reference: chr 22
allele count: 1
allele frequency: 9.046826373308244e-6
allele num: 110536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-47T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-47T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-47T>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-47T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-47T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-47T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-47T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-47T>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-47T>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-47T>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11387
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12289
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2177
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6380
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD

22-45258108-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258108
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258108
    reference: chr 22
allele count: 3
allele frequency: 2.714047911992473e-5
allele num: 110536
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-47T>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-47T>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-47T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-47T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-47T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-47T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-47T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-47T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-47T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-47T>G
  variant of: http://identifiers.org/hgnc/34512
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2377
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12385
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11387
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8663
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7820
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2177
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

22-45258110-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258110
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258110
    reference: chr 22
allele count: 1
allele frequency: 9.053214796574263e-6
allele num: 110458
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-45C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-45C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-45C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-45C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-45C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-45C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-45C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-45C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-45C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-45C>T
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7847
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9092
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2231
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

22-45258114-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258114
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258114
    reference: chr 22
allele count: 11
allele frequency: 9.939998554182029e-5
allele num: 110664
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-41T>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-41T>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-41T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-41T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-41T>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-41T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-41T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-41T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-41T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-41T>G
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11762
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9721
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7869
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2241
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3399
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

22-45258116-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258116
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258116
    reference: chr 22
allele count: 13
allele frequency: 1.174833264048295e-4
allele num: 110654
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-39G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-39G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-39G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-39G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-39G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-39G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-39G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-39G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-39G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-39G>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11836
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4793
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1458
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7888
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12678
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2682
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4917
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

22-45258117-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258117
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258117
    reference: chr 22
allele count: 1
allele frequency: 9.034892755822988e-6
allele num: 110682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-38G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-38G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-38G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-38G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-38G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-38G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-38G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-38G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-38G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-38G>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12716
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2224
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

22-45258117-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258117
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258117
    reference: chr 22
allele count: 3
allele frequency: 2.710467826746896e-5
allele num: 110682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-38G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-38G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-38G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-38G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-38G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-38G>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-38G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-38G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-38G>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-38G>C
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11870
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6575
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

22-45258118-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258118
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258118
    reference: chr 22
allele count: 1
allele frequency: 9.03326046503225e-6
allele num: 110702
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-37T>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-37T>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-37T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-37T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-37T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-37T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-37T>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-37T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-37T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-37T>C
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2685
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7903
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12768
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4948
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

22-45258119-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258119
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258119
    reference: chr 22
allele count: 2
allele frequency: 1.806032147372223e-5
allele num: 110740
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-36G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-36G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-36G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-36G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-36G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-36G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-36G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-36G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-36G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-36G>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4312
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2086
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

22-45258119-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258119
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258119
    reference: chr 22
allele count: 2
allele frequency: 1.806032147372223e-5
allele num: 110740
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-36G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-36G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-36G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-36G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-36G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-36G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-36G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-36G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-36G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-36G>T
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2684
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2554
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12803
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2157
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

22-45258122-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258122
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258122
    reference: chr 22
allele count: 1
allele frequency: 9.028367129520954e-6
allele num: 110762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-33C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-33C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-33C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-33C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-33C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-33C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-33C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-33C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-33C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-33C>T
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2750
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7942
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6627
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

22-45258126-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258126
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258126
    reference: chr 22
allele count: 1
allele frequency: 9.019572472264815e-6
allele num: 110870
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-29C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-29C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-29C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-29C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-29C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-29C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-29C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-29C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-29C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-29C>T
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4808
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14919
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

22-45258128-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258128
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258128
    reference: chr 22
allele count: 6
allele frequency: 5.40784136998648e-5
allele num: 110950
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-27C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-27C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-27C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-27C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-27C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-27C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-27C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-27C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-27C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-27C>T
  variant of: http://identifiers.org/hgnc/34512
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10096
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7975
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15011
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 1
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

22-45258128-CCTTTA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258128
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258123
    reference: chr 22
allele count: 1
allele frequency: 9.013068949977467e-6
allele num: 110950
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-23_*807-19delTACTT
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-23_1612-19delTACTT
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-23_1075-19delTACTT
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-23_1194-19delTACTT
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-23_878-19delTACTT
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-23_1348-19delTACTT
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-23_1375-19delTACTT
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-23_1612-19delTACTT
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-23_982-19delTACTT
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-23_175-19delTACTT
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4815
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2013
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3072
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7975
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2698
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2630
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3497
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: CCTTTA
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

22-45258129-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258129
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258129
    reference: chr 22
allele count: 1
allele frequency: 9.00835975785529e-6
allele num: 111008
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-26C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-26C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-26C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-26C>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-26C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-26C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-26C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-26C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-26C>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-26C>T
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4820
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10087
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7983
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12132
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1724
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

22-45258130-TTTAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258130
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258126
    reference: chr 22
allele count: 605
allele frequency: 5.445544554455445e-3
allele num: 111100
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-22_1075-19delACTT
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-22_1612-19delACTT
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-22_175-19delACTT
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-22_1375-19delACTT
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-22_1348-19delACTT
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-22_1194-19delACTT
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-22_878-19delACTT
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-22_982-19delACTT
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-22_*807-19delACTT
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-22_1612-19delACTT
  variant of: http://identifiers.org/hgnc/34512
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 5.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 5.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12102
  bin: 3.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 10064
  bin: 2.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 7970
  bin: 3.75e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 4.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 4838
  bin: 4.25e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 3186
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 13000
  bin: 2.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 6.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 47
genotype quality: GenotypeQuality
  all individuals: 5008
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1675
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 22
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: TTTAC
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/22-45258134-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258134
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258134
    reference: chr 22
allele count: 5
allele frequency: 4.542316217885824e-5
allele num: 110076
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-21C>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-21C>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-21C>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-21C>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-21C>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-21C>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-21C>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-21C>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-21C>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-21C>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4778
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12093
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4334
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13876
  bin: 9.75e1
  variant carriers: 5
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP

22-45258135-TTG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258135
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258133
    reference: chr 22
allele count: 2
allele frequency: 1.81596963698767e-5
allele num: 110134
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-13_982-12delTG
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-13_1348-12delTG
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-13_1194-12delTG
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-13_1612-12delTG
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-13_*807-12delTG
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-13_878-12delTG
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-13_1375-12delTG
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-13_1612-12delTG
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-13_1075-12delTG
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-13_175-12delTG
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12132
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1580
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1484
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: TTG
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum

22-45258136-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258136
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258136
    reference: chr 22
allele count: 1
allele frequency: 8.981820794711504e-6
allele num: 111336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-19T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-19T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-19T>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-19T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-19T>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-19T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-19T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-19T>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-19T>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-19T>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14124
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2418
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

22-45258136-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258136
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258136
    reference: chr 22
allele count: 10
allele frequency: 8.981820794711504e-5
allele num: 111336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-19T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-19T>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-19T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-19T>G
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-19T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-19T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-19T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-19T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-19T>G
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-19T>G
  variant of: http://identifiers.org/hgnc/34512
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8010
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10139
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3545
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3064
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

22-45258139-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258139
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258139
    reference: chr 22
allele count: 2
allele frequency: 1.794591102417314e-5
allele num: 111446
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-16G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-16G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-16G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-16G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-16G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-16G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-16G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-16G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-16G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-16G>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8012
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4858
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6790
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

22-45258139-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258139
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258139
    reference: chr 22
allele count: 2
allele frequency: 1.794591102417314e-5
allele num: 111446
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-16G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-16G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-16G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-16G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-16G>T
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-16G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-16G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-16G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-16G>T
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-16G>T
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8012
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10165
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1235
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3223
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

22-45258140-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258140
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258140
    reference: chr 22
allele count: 1
allele frequency: 8.97037980588098e-6
allele num: 111478
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-15T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-15T>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-15T>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-15T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-15T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-15T>C
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-15T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-15T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-15T>C
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-15T>C
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ

22-45258141-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258141
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258141
    reference: chr 22
allele count: 46
allele frequency: 4.12467271618665e-4
allele num: 111524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-14G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-14G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-14G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-14G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-14G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-14G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-14G>A
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-14G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-14G>A
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-14G>A
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13127
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8015
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4854
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12198
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 8.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3545
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

22-45258147-T-TCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 45258147
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 45258149
    reference: chr 22
allele count: 1
allele frequency: 8.942464185430938e-6
allele num: 111826
alternate allele: TCC
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374422
  ensembl transcript: ENST00000389772
  gene symbol: ARHGAP8
  hgvsc: ENST00000389772.4:c.*807-7_*807-6dupCC
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000429240
  ensembl transcript: ENST00000517296
  gene symbol: ARHGAP8
  hgvsc: ENST00000517296.3:c.1612-7_1612-6dupCC
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000354732
  ensembl transcript: ENST00000361473
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000361473.5:c.1375-7_1375-6dupCC
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374423
  ensembl transcript: ENST00000389773
  gene symbol: ARHGAP8
  hgvsc: ENST00000389773.5:c.1348-7_1348-6dupCC
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000348407
  ensembl transcript: ENST00000356099
  gene symbol: ARHGAP8
  hgvsc: ENST00000356099.6:c.982-7_982-6dupCC
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000337287
  ensembl transcript: ENST00000336963
  gene symbol: ARHGAP8
  hgvsc: ENST00000336963.4:c.878-7_878-6dupCC
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000262731
  ensembl transcript: ENST00000352766
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000352766.7:c.1612-7_1612-6dupCC
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000248405
  ensembl protein: ENSP00000425026
  ensembl transcript: ENST00000515632
  gene symbol: PRR5-ARHGAP8
  hgvsc: ENST00000515632.1:c.1194-7_1194-6dupCC
  variant of: http://identifiers.org/hgnc/34512
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl transcript: ENST00000469342
  gene symbol: ARHGAP8
  hgvsc: ENST00000469342.1:n.175-7_175-6dupCC
  variant of: http://identifiers.org/hgnc/677
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000241484
  ensembl protein: ENSP00000374424
  ensembl transcript: ENST00000389774
  gene symbol: ARHGAP8
  hgvsc: ENST00000389774.2:c.1075-7_1075-6dupCC
  variant of: http://identifiers.org/hgnc/677
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2742
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3812
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
hgvs: c.1348-7_1348-6dupCC
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 1162
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1458
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6426
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30951
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1620
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3538
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1600
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1181
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 955
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3362
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2074
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.946290033817386e-5
allele num: 10054
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15780
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.015e0

FS
type: SiteQuality
SIO_000300: 9.66e-1

MQ
type: SiteQuality
SIO_000300: 5.868e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.76e-1

QD
type: SiteQuality
SIO_000300: 2.266e1

VQSLOD
type: SiteQuality
SIO_000300: -1.342e0

DP
type: SiteQuality
SIO_000300: 1.575657e6

GenotypeQuality
all individuals: 648
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31620
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1181
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2443
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3565
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 7.5e0
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GenotypeQuality
all individuals: 1602
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1449
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1197
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6433
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3379
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 1130
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2065
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.813678829543451e-5
allele num: 11346
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.372578923288089e-4
allele num: 65570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.687576875768758e-4
allele num: 6504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.333122229259025e-5
allele num: 15790
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.531e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.64e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.861e1

VQSLOD
type: SiteQuality
SIO_000300: -9.88e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

DP
type: SiteQuality
SIO_000300: 1.574868e6

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.52e-1

GenotypeQuality
all individuals: 1525
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1434
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 1610
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6420
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10060
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8474
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.526810797605961e-5
allele num: 65496
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15774
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.896e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

FS
type: SiteQuality
SIO_000300: 1.0296e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.93e-1

QD
type: SiteQuality
SIO_000300: 1.51e1

MQRankSum
type: SiteQuality
SIO_000300: 5.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e-1

DP
type: SiteQuality
SIO_000300: 1.569994e6

GenotypeQuality
all individuals: 79
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1183
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1610
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 88
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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
all individuals: 3365
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2059
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10052
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11314
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.360513929525506e-5
allele num: 15722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65444
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.07e-1

MQ
type: SiteQuality
SIO_000300: 6.005e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

FS
type: SiteQuality
SIO_000300: 3.161e0

QD
type: SiteQuality
SIO_000300: 3.99e0

DP
type: SiteQuality
SIO_000300: 1.566249e6

VQSLOD
type: SiteQuality
SIO_000300: 4.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e-1

GenotypeQuality
all individuals: 3365
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2059
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
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variant carriers: 0

GenotypeQuality
all individuals: 687
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1610
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variant carriers: 0

GenotypeQuality
all individuals: 1183
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 23
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GenotypeQuality
all individuals: 1283
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variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 2463
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variant carriers: 0

GenotypeQuality
all individuals: 1236
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3892
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8466
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10052
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.360513929525506e-5
allele num: 15722
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65444
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e-1

QD
type: SiteQuality
SIO_000300: 3.99e0

MQ
type: SiteQuality
SIO_000300: 6.005e1

MQRankSum
type: SiteQuality
SIO_000300: -3.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

FS
type: SiteQuality
SIO_000300: 3.161e0

DP
type: SiteQuality
SIO_000300: 1.566249e6

VQSLOD
type: SiteQuality
SIO_000300: 4.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
all individuals: 23355
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 158
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19964
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
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variant carriers: 0

GenotypeQuality
all individuals: 3948
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3848
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
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variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1459
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15694
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.537609939110646e-5
allele num: 65036
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11150
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.04e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.559e0

DP
type: SiteQuality
SIO_000300: 1.818284e6

MQ
type: SiteQuality
SIO_000300: 5.866e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e-1

QD
type: SiteQuality
SIO_000300: 1.641e1

GenotypeQuality
all individuals: 359
bin: 4.25e1
variant carriers: 44

GenotypeQuality
all individuals: 23355
bin: 9.75e1
variant carriers: 22274

GenotypeQuality
all individuals: 158
bin: 1.75e1
variant carriers: 24

GenotypeQuality
all individuals: 1459
bin: 3.25e1
variant carriers: 48

GenotypeQuality
all individuals: 112
bin: 1.25e1
variant carriers: 19

GenotypeQuality
all individuals: 1154
bin: 7.75e1
variant carriers: 210

GenotypeQuality
all individuals: 176
bin: 2.5e0
variant carriers: 19

GenotypeQuality
all individuals: 837
bin: 8.25e1
variant carriers: 247

GenotypeQuality
all individuals: 473
bin: 5.25e1
variant carriers: 112

GenotypeQuality
all individuals: 19964
bin: 6.25e1
variant carriers: 137

GenotypeQuality
all individuals: 1046
bin: 7.25e1
variant carriers: 112

GenotypeQuality
all individuals: 522
bin: 9.25e1
variant carriers: 212

GenotypeQuality
all individuals: 3948
bin: 2.25e1
variant carriers: 48

GenotypeQuality
all individuals: 348
bin: 8.75e1
variant carriers: 122

GenotypeQuality
all individuals: 342
bin: 5.75e1
variant carriers: 100

GenotypeQuality
all individuals: 3848
bin: 6.75e1
variant carriers: 178

GenotypeQuality
all individuals: 1192
bin: 2.75e1
variant carriers: 34

South Asian
type: Population
allele count: 2047
allele frequency: 1.304320122339748e-1
allele num: 15694
num of homozygotes: 162

African
type: Population
allele count: 890
allele frequency: 8.866308029487946e-2
allele num: 10038
num of homozygotes: 39

Latino
type: Population
allele count: 3558
allele frequency: 3.191031390134529e-1
allele num: 11150
num of homozygotes: 545

European (Non-Finnish)
type: Population
allele count: 16318
allele frequency: 2.509071898640753e-1
allele num: 65036
num of homozygotes: 2021

Other
type: Population
allele count: 218
allele frequency: 2.505747126436781e-1
allele num: 870
num of homozygotes: 29

East Asian
type: Population
allele count: 1899
allele frequency: 2.263948497854077e-1
allele num: 8388
num of homozygotes: 219

European (Finnish)
type: Population
allele count: 2604
allele frequency: 4.038461538461539e-1
allele num: 6448
num of homozygotes: 518

DP
type: SiteQuality
SIO_000300: 1.818284e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.04e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.559e0

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

QD
type: SiteQuality
SIO_000300: 1.641e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

MQ
type: SiteQuality
SIO_000300: 5.866e1

GenotypeQuality
all individuals: 176
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3948
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1046
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GenotypeQuality
all individuals: 342
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GenotypeQuality
all individuals: 139
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GenotypeQuality
all individuals: 348
bin: 8.75e1
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GenotypeQuality
all individuals: 882
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 473
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19964
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 522
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11150
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.962143853357243e-5
allele num: 10038
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65036
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15694
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.866e1

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.559e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.04e-2

DP
type: SiteQuality
SIO_000300: 1.818284e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

QD
type: SiteQuality
SIO_000300: 1.641e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e-1

GenotypeQuality
all individuals: 1850
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 8.75e1
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GenotypeQuality
all individuals: 582
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
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variant carriers: 0

GenotypeQuality
all individuals: 26
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GenotypeQuality
all individuals: 133
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GenotypeQuality
all individuals: 1194
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GenotypeQuality
all individuals: 3231
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GenotypeQuality
all individuals: 5739
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GenotypeQuality
all individuals: 75
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GenotypeQuality
all individuals: 541
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GenotypeQuality
all individuals: 2353
bin: 2.75e1
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GenotypeQuality
all individuals: 2334
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variant carriers: 1

GenotypeQuality
all individuals: 1071
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GenotypeQuality
all individuals: 1894
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variant carriers: 0

GenotypeQuality
all individuals: 1518
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1610
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9950
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551494088807522e-5
allele num: 64454
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11030
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.299999999999999e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.938e0

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.437e-1

QD
type: SiteQuality
SIO_000300: 1.261e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.08e-1

DP
type: SiteQuality
SIO_000300: 1.473361e6

MQ
type: SiteQuality
SIO_000300: 5.796e1

GenotypeQuality
all individuals: 1194
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1518
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28192
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1850
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2353
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7051
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3231
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1610
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 5739
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2334
bin: 9.75e1
variant carriers: 86

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8326
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.813236627379873e-4
allele num: 11030
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

African
type: Population
allele count: 84
allele frequency: 8.442211055276382e-3
allele num: 9950
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.654482266422565e-5
allele num: 64454
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.47836227001814e-5
allele num: 15436
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.938e0

VQSLOD
type: SiteQuality
SIO_000300: -1.437e-1

QD
type: SiteQuality
SIO_000300: 1.261e1

MQ
type: SiteQuality
SIO_000300: 5.796e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.299999999999999e-3

DP
type: SiteQuality
SIO_000300: 1.473361e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.08e-1

GenotypeQuality
all individuals: 133
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5739
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1894
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28192
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1850
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1518
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2334
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 159
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1194
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1610
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3231
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7051
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.010050251256281e-4
allele num: 9950
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6380
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.066183136899366e-5
allele num: 11030
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.201056930098487e-4
allele num: 8326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.861792906569026e-4
allele num: 64454
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15436
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.938e0

DP
type: SiteQuality
SIO_000300: 1.473361e6

MQRankSum
type: SiteQuality
SIO_000300: 3.13e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.261e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.299999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.437e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.08e-1

MQ
type: SiteQuality
SIO_000300: 5.796e1

GenotypeQuality
all individuals: 72
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1828
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29268
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2235
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 116
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5713
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1876
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1195
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1594
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7149
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3217
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.012882447665056e-4
allele num: 9936
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15454
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.066183136899366e-5
allele num: 11030
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.551253412757508e-5
allele num: 64464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6368
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.467523e6

QD
type: SiteQuality
SIO_000300: 1.09e1

FS
type: SiteQuality
SIO_000300: 3.552e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 5.858e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.156e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.52e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.3e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.247e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

GenotypeQuality
all individuals: 3163
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1824
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1553
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2338
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1770
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30121
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7177
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 481
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2624
bin: 9.75e1
variant carriers: 272

GenotypeQuality
all individuals: 340
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15444
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.004811547714515e-4
allele num: 9976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 45
allele frequency: 7.062146892655367e-3
allele num: 6372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 226
allele frequency: 3.507138423339541e-3
allele num: 64440
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8330
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.069472156720479e-5
allele num: 11026
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.463904e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.12e-2

QD
type: SiteQuality
SIO_000300: 1.659e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.908e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.14e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.02e-1

GenotypeQuality
all individuals: 1770
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 495
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1553
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1824
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2624
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2338
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 99
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30121
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7177
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1166
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 9.069472156720479e-5
allele num: 11026
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9976
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6372
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64440
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.908e1

DP
type: SiteQuality
SIO_000300: 1.463904e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.12e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.71e0

QD
type: SiteQuality
SIO_000300: 1.659e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.14e-1

GenotypeQuality
all individuals: 1166
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30121
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1770
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3163
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7177
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1824
bin: 7.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 481
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2624
bin: 9.75e1
variant carriers: 222

GenotypeQuality
all individuals: 124
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2338
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5611
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 649
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 214
allele frequency: 2.145148356054531e-2
allele num: 9976
num of homozygotes: 3

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6372
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.475006475006475e-5
allele num: 15444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.207324643078833e-5
allele num: 64440
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8330
num of homozygotes: 0

Latino
type: Population
allele count: 10
allele frequency: 9.069472156720479e-4
allele num: 11026
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

MQ
type: SiteQuality
SIO_000300: 5.908e1

MQRankSum
type: SiteQuality
SIO_000300: 5.39e-1

QD
type: SiteQuality
SIO_000300: 1.659e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.12e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.14e-1

DP
type: SiteQuality
SIO_000300: 1.463904e6

GenotypeQuality
all individuals: 5450
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3791
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28307
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2177
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 7957
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2763
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15340
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.61969111969112e-4
allele num: 8288
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10988
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6354
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.033071183706392e-4
allele num: 9918
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64254
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.42e-1

MQ
type: SiteQuality
SIO_000300: 5.884e1

QD
type: SiteQuality
SIO_000300: 1.407e1

VQSLOD
type: SiteQuality
SIO_000300: 1.0e-1

FS
type: SiteQuality
SIO_000300: 7.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.15e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.943e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e-1

DP
type: SiteQuality
SIO_000300: 1.42693e6

GenotypeQuality
all individuals: 28307
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3791
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 168
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2177
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1505
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7957
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64254
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9918
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.640334910811795e-4
allele num: 10988
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8288
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15340
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.0e-1

DP
type: SiteQuality
SIO_000300: 1.42693e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.943e0

MQ
type: SiteQuality
SIO_000300: 5.884e1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e-1

FS
type: SiteQuality
SIO_000300: 7.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.15e-2

QD
type: SiteQuality
SIO_000300: 1.407e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.83e-1

GenotypeQuality
all individuals: 469
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1744
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3195
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4515
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5271
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1470
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25791
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1148
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2167
bin: 9.75e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8266
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15294
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.125752874612155e-5
allele num: 10958
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6344
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64084
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.33e0

MQ
type: SiteQuality
SIO_000300: 5.906e1

FS
type: SiteQuality
SIO_000300: 7.57e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

DP
type: SiteQuality
SIO_000300: 1.393181e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.27e-1

QD
type: SiteQuality
SIO_000300: 1.138e1

GenotypeQuality
all individuals: 19831
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 7.5e0
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6055
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 9.75e1
variant carriers: 2

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 848
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15124
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.135779241141423e-5
allele num: 63780
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.462e0

VQSLOD
type: SiteQuality
SIO_000300: 3.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQ
type: SiteQuality
SIO_000300: 5.917e1

FS
type: SiteQuality
SIO_000300: 6.054e0

MQRankSum
type: SiteQuality
SIO_000300: 4.86e-1

QD
type: SiteQuality
SIO_000300: 1.591e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-2

DP
type: SiteQuality
SIO_000300: 1.32719e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.93e-1

GenotypeQuality
all individuals: 1113
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1621
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variant carriers: 0

GenotypeQuality
all individuals: 1260
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variant carriers: 0

GenotypeQuality
all individuals: 4083
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1353
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 1.25e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 915
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3940
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1261
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6030
bin: 3.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6320
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10862
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15092
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63694
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9824
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.182033096926714e-3
allele num: 846
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.41e0

VQSLOD
type: SiteQuality
SIO_000300: -7.731e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.798e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

DP
type: SiteQuality
SIO_000300: 1.324665e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.7e-1

MQ
type: SiteQuality
SIO_000300: 5.901e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.11e-1

GenotypeQuality
all individuals: 1572
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 390
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variant carriers: 0

GenotypeQuality
all individuals: 1220
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variant carriers: 0

GenotypeQuality
all individuals: 4860
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variant carriers: 0

GenotypeQuality
all individuals: 9709
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variant carriers: 0

GenotypeQuality
all individuals: 6526
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variant carriers: 0

GenotypeQuality
all individuals: 4149
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variant carriers: 0

GenotypeQuality
all individuals: 1088
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variant carriers: 0

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
all individuals: 369
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GenotypeQuality
all individuals: 798
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variant carriers: 0

GenotypeQuality
all individuals: 2152
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3788
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19038
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1540
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.853911753800519e-4
allele num: 10788
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6268
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14902
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.577535888941474e-5
allele num: 63390
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8156
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.41e-1

FS
type: SiteQuality
SIO_000300: 6.164e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

DP
type: SiteQuality
SIO_000300: 1.29937e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.642e0

QD
type: SiteQuality
SIO_000300: 1.505e1

GenotypeQuality
all individuals: 72
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1685
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3737
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1567
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variant carriers: 0

GenotypeQuality
all individuals: 18104
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variant carriers: 0

GenotypeQuality
all individuals: 1211
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variant carriers: 0

GenotypeQuality
all individuals: 4238
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
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variant carriers: 0

GenotypeQuality
all individuals: 649
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6721
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1769
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14930
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.577237311125832e-5
allele num: 63402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.004e0

MQ
type: SiteQuality
SIO_000300: 5.82e1

VQSLOD
type: SiteQuality
SIO_000300: -7.288e-1

DP
type: SiteQuality
SIO_000300: 1.28931e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.377e0

QD
type: SiteQuality
SIO_000300: 1.224e1

GenotypeQuality
all individuals: 1685
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9765
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 836
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5146
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
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variant carriers: 0

GenotypeQuality
all individuals: 4238
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 3737
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 8.75e1
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GenotypeQuality
all individuals: 2151
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1769
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 445
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variant carriers: 0

GenotypeQuality
all individuals: 1211
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10800
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63402
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6270
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.697923643670462e-5
allele num: 14930
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.224e1

FS
type: SiteQuality
SIO_000300: 1.004e0

DP
type: SiteQuality
SIO_000300: 1.28931e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.377e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.288e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.58e-1

MQ
type: SiteQuality
SIO_000300: 5.82e1

GenotypeQuality
all individuals: 6966
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.5e0
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GenotypeQuality
all individuals: 3575
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2001
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 454
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variant carriers: 1

GenotypeQuality
all individuals: 1938
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1039
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variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 4336
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16160
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1187
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1541
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1070
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2285
bin: 9.75e1
variant carriers: 151

African
type: Population
allele count: 2
allele frequency: 2.048760499897562e-4
allele num: 9762
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.860119047619048e-4
allele num: 10752
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.187648456057007e-3
allele num: 842
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8088
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.404098623118795e-4
allele num: 6246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 146
allele frequency: 2.310345918916353e-3
allele num: 63194
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.34752728742757e-4
allele num: 14842
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.826e1

DP
type: SiteQuality
SIO_000300: 1.276661e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

QD
type: SiteQuality
SIO_000300: 1.196e1

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.355e0

GenotypeQuality
all individuals: 1918
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1185
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.5e0
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GenotypeQuality
all individuals: 2140
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5534
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6982
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
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variant carriers: 0

GenotypeQuality
all individuals: 16829
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
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variant carriers: 0

GenotypeQuality
all individuals: 4356
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9798
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 5.25e1
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GenotypeQuality
all individuals: 648
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3595
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1070
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9764
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.720430107526882e-5
allele num: 14880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6242
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63246
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10746
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8104
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.89e0

MQ
type: SiteQuality
SIO_000300: 5.741e1

FS
type: SiteQuality
SIO_000300: 3.938e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.259e0

QD
type: SiteQuality
SIO_000300: 1.283e1

DP
type: SiteQuality
SIO_000300: 1.274421e6

MQRankSum
type: SiteQuality
SIO_000300: 7.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

GenotypeQuality
all individuals: 2049
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7088
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1532
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.025641025641026e-4
allele num: 9750
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8090
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6244
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14910
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63210
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.896e1

DP
type: SiteQuality
SIO_000300: 1.268775e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.783e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

FS
type: SiteQuality
SIO_000300: 9.536e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.59e0

QD
type: SiteQuality
SIO_000300: 1.606e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

GenotypeQuality
all individuals: 460
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6047
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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: 4.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63032
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6242
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8064
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.741270055278414e-5
allele num: 14834
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.23e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e-1

MQ
type: SiteQuality
SIO_000300: 5.919e1

MQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

DP
type: SiteQuality
SIO_000300: 1.259133e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

FS
type: SiteQuality
SIO_000300: 1.399e0

QD
type: SiteQuality
SIO_000300: 1.322e1

GenotypeQuality
all individuals: 406
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4468
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10658
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6234
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.588259585146596e-5
allele num: 62962
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8058
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.756756756756757e-5
allele num: 14800
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.258295e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.447e0

FS
type: SiteQuality
SIO_000300: 3.117e0

VQSLOD
type: SiteQuality
SIO_000300: -1.894e0

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.777e1

QD
type: SiteQuality
SIO_000300: 1.332e1

GenotypeQuality
all individuals: 9696
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7296
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1504
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 554
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variant carriers: 0

GenotypeQuality
all individuals: 1159
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 446
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variant carriers: 0

GenotypeQuality
all individuals: 2509
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2137
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1057
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
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variant carriers: 0

GenotypeQuality
all individuals: 4504
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8044
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.02880658436214e-4
allele num: 9720
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14748
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: 62800
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e0

VQSLOD
type: SiteQuality
SIO_000300: -2.361e0

MQRankSum
type: SiteQuality
SIO_000300: 1.78e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.61e-1

MQ
type: SiteQuality
SIO_000300: 5.855e1

DP
type: SiteQuality
SIO_000300: 1.253029e6

QD
type: SiteQuality
SIO_000300: 1.144e1

GenotypeQuality
all individuals: 648
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2888
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
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variant carriers: 0

GenotypeQuality
all individuals: 659
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3135
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variant carriers: 0

GenotypeQuality
all individuals: 2135
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.851192107426693e-5
allele num: 14596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62478
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6192
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7976
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

VQSLOD
type: SiteQuality
SIO_000300: 4.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-1

QD
type: SiteQuality
SIO_000300: 1.192e1

MQRankSum
type: SiteQuality
SIO_000300: 4.56e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.74e-1

FS
type: SiteQuality
SIO_000300: 7.084e0

DP
type: SiteQuality
SIO_000300: 1.237485e6

GenotypeQuality
all individuals: 6912
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9965
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variant carriers: 0

GenotypeQuality
all individuals: 169
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.25e1
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GenotypeQuality
all individuals: 2132
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8832
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.612851198348441e-5
allele num: 62002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6154
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14368
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.946e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 1.22936e6

MQ
type: SiteQuality
SIO_000300: 5.82e1

VQSLOD
type: SiteQuality
SIO_000300: 1.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-1

GenotypeQuality
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bin: 4.25e1
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
all individuals: 2133
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1111
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7834
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6138
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.615665492616409e-5
allele num: 61894
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.084e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.704e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

QD
type: SiteQuality
SIO_000300: 1.651e1

MQRankSum
type: SiteQuality
SIO_000300: 1.49e0

DP
type: SiteQuality
SIO_000300: 1.227737e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.46e0

GenotypeQuality
all individuals: 797
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3250
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4579
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 713
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variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8200
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3200
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2816
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8292
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1709
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6952
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 449
bin: 8.75e1
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GenotypeQuality
all individuals: 1027
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GenotypeQuality
all individuals: 4979
bin: 4.75e1
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GenotypeQuality
all individuals: 2159
bin: 9.75e1
variant carriers: 35

GenotypeQuality
all individuals: 551
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1083
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 29
allele frequency: 3.71604305484367e-3
allele num: 7804
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.013606396409034e-5
allele num: 14258
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.866653688923497e-5
allele num: 61644
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.059322033898305e-4
allele num: 9440
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6108
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.940240589833139e-4
allele num: 10308
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.377e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.739e1

QD
type: SiteQuality
SIO_000300: 1.357e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e-1

DP
type: SiteQuality
SIO_000300: 1.226429e6

VQSLOD
type: SiteQuality
SIO_000300: -5.647e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 7656
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5129
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 8

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1468
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9306
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13988
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.636875531984548e-5
allele num: 61092
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6058
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

East Asian
type: Population
allele count: 5
allele frequency: 6.481721545242416e-4
allele num: 7714
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.293e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

FS
type: SiteQuality
SIO_000300: 3.064e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.49e0

MQ
type: SiteQuality
SIO_000300: 5.808e1

DP
type: SiteQuality
SIO_000300: 1.225286e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

QD
type: SiteQuality
SIO_000300: 1.45e1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 449
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variant carriers: 0

GenotypeQuality
all individuals: 828
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9306
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.910626595953644e-5
allele num: 61092
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7714
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6058
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13988
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.49e0

FS
type: SiteQuality
SIO_000300: 3.064e0

MQ
type: SiteQuality
SIO_000300: 5.808e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.293e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

DP
type: SiteQuality
SIO_000300: 1.225286e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

QD
type: SiteQuality
SIO_000300: 1.45e1

GenotypeQuality
all individuals: 1537
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

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
all individuals: 4192
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variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.422475106685633e-4
allele num: 14060
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10118
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61100
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7716
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6044
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.225412e6

VQSLOD
type: SiteQuality
SIO_000300: -6.076e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.652e0

MQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

MQ
type: SiteQuality
SIO_000300: 5.85e1

FS
type: SiteQuality
SIO_000300: 5.944e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

QD
type: SiteQuality
SIO_000300: 1.268e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

GenotypeQuality
all individuals: 7670
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5125
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 815
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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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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4192
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2138
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.636661211129296e-5
allele num: 61100
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10118
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7716
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.070663811563169e-4
allele num: 9340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14060
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6044
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.23e-1

FS
type: SiteQuality
SIO_000300: 5.944e0

VQSLOD
type: SiteQuality
SIO_000300: -6.076e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.652e0

MQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

QD
type: SiteQuality
SIO_000300: 1.268e1

DP
type: SiteQuality
SIO_000300: 1.225412e6

MQ
type: SiteQuality
SIO_000300: 5.85e1

GenotypeQuality
all individuals: 1487
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7596
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3282
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.069976460517869e-4
allele num: 9346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7748
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.63036389722186e-5
allele num: 61336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14148
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

DP
type: SiteQuality
SIO_000300: 1.225641e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

FS
type: SiteQuality
SIO_000300: 1.2227e1

VQSLOD
type: SiteQuality
SIO_000300: -1.421e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

QD
type: SiteQuality
SIO_000300: 1.443e1

MQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

MQ
type: SiteQuality
SIO_000300: 5.85e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-2

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6082
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7748
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14148
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.63036389722186e-5
allele num: 61336
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.421e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

DP
type: SiteQuality
SIO_000300: 1.225641e6

MQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.2227e1

MQ
type: SiteQuality
SIO_000300: 5.85e1

QD
type: SiteQuality
SIO_000300: 1.443e1

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9436
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9096
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.565876421032852e-5
allele num: 63862
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.07e-1

DP
type: SiteQuality
SIO_000300: 1.824469e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.075e0

VQSLOD
type: SiteQuality
SIO_000300: 4.76e0

QD
type: SiteQuality
SIO_000300: 1.807e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 254

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1054
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variant carriers: 1

GenotypeQuality
all individuals: 2090
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variant carriers: 0

Latino
type: Population
allele count: 8
allele frequency: 7.016312927556569e-4
allele num: 11402
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.525252525252525e-3
allele num: 792
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 71
allele frequency: 1.112294773781176e-3
allele num: 63832
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.518372304889159e-4
allele num: 6586
num of homozygotes: 0

African
type: Population
allele count: 168
allele frequency: 1.780415430267062e-2
allele num: 9436
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 5.502971604666519e-4
allele num: 9086
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8494
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

QD
type: SiteQuality
SIO_000300: 1.514e1

VQSLOD
type: SiteQuality
SIO_000300: 5.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

DP
type: SiteQuality
SIO_000300: 1.827647e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

GenotypeQuality
all individuals: 848
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3363
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 901
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13819
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 1161
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11398
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6206
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1184
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2116
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 608
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4768
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2271
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.097694840834248e-4
allele num: 9110
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.761170492377782e-5
allele num: 11414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.25250501002004e-4
allele num: 63872
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

DP
type: SiteQuality
SIO_000300: 1.830779e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.89e-1

FS
type: SiteQuality
SIO_000300: 3.168e0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

QD
type: SiteQuality
SIO_000300: 1.455e1

GenotypeQuality
all individuals: 848
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1184
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 361
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variant carriers: 0

GenotypeQuality
all individuals: 2271
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.058425063505504e-4
allele num: 9448
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9110
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.56563126252505e-5
allele num: 63872
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

QD
type: SiteQuality
SIO_000300: 1.455e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.72e-1

DP
type: SiteQuality
SIO_000300: 1.830779e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.168e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.89e-1

GenotypeQuality
all individuals: 4113
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11398
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2271
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 901
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1344
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 13819
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 3322
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4768
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3363
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.25250501002004e-4
allele num: 63872
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.72e-1

FS
type: SiteQuality
SIO_000300: 3.168e0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.455e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.35e0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

DP
type: SiteQuality
SIO_000300: 1.830779e6

GenotypeQuality
all individuals: 558
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3381
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4166
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variant carriers: 0

GenotypeQuality
all individuals: 1276
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variant carriers: 0

GenotypeQuality
all individuals: 209
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variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13904
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2306
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variant carriers: 0

GenotypeQuality
all individuals: 3414
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4859
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variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 792
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10176
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564896247378799e-5
allele num: 63902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

DP
type: SiteQuality
SIO_000300: 1.83535e6

FS
type: SiteQuality
SIO_000300: 1.233e0

QD
type: SiteQuality
SIO_000300: 1.372e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.75e-1

GenotypeQuality
all individuals: 4859
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 833
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 552
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variant carriers: 0

GenotypeQuality
all individuals: 1276
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
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variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3414
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 809
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13904
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1118
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4166
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3381
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variant carriers: 0

GenotypeQuality
all individuals: 12289
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6380
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variant carriers: 0

GenotypeQuality
all individuals: 2306
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9116
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10176
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.516990291262136e-4
allele num: 6592
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.129792494757598e-5
allele num: 63902
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.75e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.62e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.372e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

FS
type: SiteQuality
SIO_000300: 1.233e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.91e0

DP
type: SiteQuality
SIO_000300: 1.83535e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-2

GenotypeQuality
all individuals: 499
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13895
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 634
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2317
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variant carriers: 0

GenotypeQuality
all individuals: 4183
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variant carriers: 0

GenotypeQuality
all individuals: 6408
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variant carriers: 0

GenotypeQuality
all individuals: 345
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 544
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 738
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9130
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564504521418067e-5
allele num: 63918
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.97e0

DP
type: SiteQuality
SIO_000300: 1.84265e6

FS
type: SiteQuality
SIO_000300: 2.363e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.81e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.248e1

GenotypeQuality
all individuals: 6542
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4916
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14111
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
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variant carriers: 0

GenotypeQuality
all individuals: 522
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variant carriers: 0

GenotypeQuality
all individuals: 1795
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variant carriers: 0

GenotypeQuality
all individuals: 655
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variant carriers: 0

GenotypeQuality
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variant carriers: 11

GenotypeQuality
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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: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2359
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.727526618956188e-5
allele num: 11458
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.563721657544957e-5
allele num: 63950
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10186
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 9.823182711198428e-4
allele num: 9162
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.94e-1

DP
type: SiteQuality
SIO_000300: 1.852797e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.775e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.91e-1

FS
type: SiteQuality
SIO_000300: 5.621e0

QD
type: SiteQuality
SIO_000300: 1.473e1

GenotypeQuality
all individuals: 2240
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1915
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14292
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6535
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variant carriers: 0

GenotypeQuality
all individuals: 13939
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 614
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variant carriers: 0

GenotypeQuality
all individuals: 437
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GenotypeQuality
all individuals: 3405
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variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 4.75e1
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GenotypeQuality
all individuals: 130
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GenotypeQuality
all individuals: 149
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GenotypeQuality
all individuals: 2368
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GenotypeQuality
all individuals: 409
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GenotypeQuality
all individuals: 252
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GenotypeQuality
all individuals: 3487
bin: 9.25e1
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GenotypeQuality
all individuals: 4264
bin: 8.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

African
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allele count: 6
allele frequency: 5.897385492431689e-4
allele num: 10174
num of homozygotes: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.094707869385713e-4
allele num: 63944
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9168
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 count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

QD
type: SiteQuality
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MQ
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VQSLOD
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MQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

FS
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SIO_000300: 2.05e0

ReadPosRankSum
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SIO_000300: 7.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.143e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.85e-1

DP
type: SiteQuality
SIO_000300: 1.856684e6

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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9174
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.563477173233271e-5
allele num: 63960
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-1

MQRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQ
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.85853e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.66e-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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variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.690431519699812e-5
allele num: 63960
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.563135023603339e-5
allele num: 63974
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9180
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e0

QD
type: SiteQuality
SIO_000300: 1.299e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.01e-1

DP
type: SiteQuality
SIO_000300: 1.860542e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.05e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.28e-1

GenotypeQuality
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variant carriers: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10180
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63980
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.34796900680911e-4
allele num: 8518
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -4.9e-2

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1.086720278200391e-4
allele num: 9202
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11466
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.562988433885589e-5
allele num: 63980
num of homozygotes: 0

African
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Other
type: Population
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allele frequency: 0.0e0
allele num: 800
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11466
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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South Asian
type: Population
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African
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allele frequency: 9.83477576711251e-5
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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

East Asian
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QD
type: SiteQuality
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DP
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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VQSLOD
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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num of homozygotes: 0

Latino
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East Asian
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European (Finnish)
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South Asian
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African
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European (Non-Finnish)
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allele frequency: 1.561572816140417e-5
allele num: 64038
num of homozygotes: 0

FS
type: SiteQuality
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MQ
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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DP
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MQRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3497
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 3.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 6.422607578676942e-4
allele num: 9342
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64048
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 3.889e0

MQ
type: SiteQuality
SIO_000300: 5.935e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.123e0

DP
type: SiteQuality
SIO_000300: 1.876043e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.72e-1

QD
type: SiteQuality
SIO_000300: 1.482e1

GenotypeQuality
all individuals: 333
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13977
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 176
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1784
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4344
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2410
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5022
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3531
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15011
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6727
bin: 6.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.561329003247564e-5
allele num: 64048
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

FS
type: SiteQuality
SIO_000300: 3.889e0

DP
type: SiteQuality
SIO_000300: 1.876043e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQ
type: SiteQuality
SIO_000300: 5.935e1

QD
type: SiteQuality
SIO_000300: 1.482e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.123e0

VQSLOD
type: SiteQuality
SIO_000300: 1.97e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.72e-1

GenotypeQuality
all individuals: 126
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3498
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13975
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2713
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2412
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15030
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6728
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4345
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5029
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3531
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9364
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8536
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.718395815170009e-5
allele num: 11470
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64076
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.35e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.719e0

VQSLOD
type: SiteQuality
SIO_000300: 8.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.338e0

MQRankSum
type: SiteQuality
SIO_000300: 1.4e-2

FS
type: SiteQuality
SIO_000300: 1.535e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
SIO_000300: 1.87736e6

GenotypeQuality
all individuals: 3494
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 218
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 14906
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 107
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 2.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 289
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6694
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2395
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3510
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 14431
bin: 9.75e1
variant carriers: 573

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4329
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2720
bin: 2.25e1
variant carriers: 1

African
type: Population
allele count: 575
allele frequency: 5.632836990595611e-2
allele num: 10208
num of homozygotes: 22

South Asian
type: Population
allele count: 2
allele frequency: 2.130379207498935e-4
allele num: 9388
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.25e-3
allele num: 800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.801529099703542e-5
allele num: 64090
num of homozygotes: 0

Latino
type: Population
allele count: 22
allele frequency: 1.918047079337402e-3
allele num: 11470
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.88851e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.65e0

MQRankSum
type: SiteQuality
SIO_000300: -3.117e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

FS
type: SiteQuality
SIO_000300: 6.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

MQ
type: SiteQuality
SIO_000300: 5.364e1

QD
type: SiteQuality
SIO_000300: 1.124e1

GenotypeQuality
all individuals: 1503
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15027
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6722
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2964
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2399
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3505
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5013
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3511
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9438
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9160
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.119832776963155e-5
allele num: 64106
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.625131256562828e-4
allele num: 11428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

VQSLOD
type: SiteQuality
SIO_000300: 2.52e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.249e1

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.647e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

DP
type: SiteQuality
SIO_000300: 1.861349e6

GenotypeQuality
all individuals: 235
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2401
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2969
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5019
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6723
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3507
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13863
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 91
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4335
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15026
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3512
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9110
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.118567953595709e-5
allele num: 64132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9518
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.892905e6

VQSLOD
type: SiteQuality
SIO_000300: 3.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

FS
type: SiteQuality
SIO_000300: 8.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.79e1

MQ
type: SiteQuality
SIO_000300: 6.114e1

MQRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

GenotypeQuality
all individuals: 236
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3064
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1384
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15162
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3544
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4369
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6782
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3545
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5077
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.559040878051823e-5
allele num: 64142
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

QD
type: SiteQuality
SIO_000300: 1.647e1

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-2

FS
type: SiteQuality
SIO_000300: 1.439e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-2

DP
type: SiteQuality
SIO_000300: 1.886465e6

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1384
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6782
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15162
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4369
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5077
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2418
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3544
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14124
bin: 9.75e1
variant carriers: 10

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.047339757017176e-4
allele num: 9548
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.40313679024664e-4
allele num: 64142
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e0

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 1.439e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.647e1

DP
type: SiteQuality
SIO_000300: 1.886465e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
all individuals: 204
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 237
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2418
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3546
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15220
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1235
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3223
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4374
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3546
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5083
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14125
bin: 9.75e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64184
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.713837574067619e-5
allele num: 11476
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.041449697979588e-4
allele num: 9602
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.422e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

DP
type: SiteQuality
SIO_000300: 1.888536e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 5.021e0

QD
type: SiteQuality
SIO_000300: 1.04e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

GenotypeQuality
all individuals: 3546
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 195
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3546
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5083
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2418
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14125
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 15220
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6790
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4374
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.169590643274854e-4
allele num: 8550
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55802069051477e-5
allele num: 64184
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.422e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

DP
type: SiteQuality
SIO_000300: 1.888536e6

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.05e-1

FS
type: SiteQuality
SIO_000300: 5.021e0

QD
type: SiteQuality
SIO_000300: 1.04e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

GenotypeQuality
all individuals: 197
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6793
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3548
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1179
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5081
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2418
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4372
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15223
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3550
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14115
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.712319219376198e-5
allele num: 11478
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9630
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

DP
type: SiteQuality
SIO_000300: 1.889347e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.608e0

FS
type: SiteQuality
SIO_000300: 1.429e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.76e0

MQRankSum
type: SiteQuality
SIO_000300: -2.51e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.207e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.47e-1

QD
type: SiteQuality
SIO_000300: 1.248e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 15242
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4371
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5082
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2415
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3275
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6794
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3546
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14141
bin: 9.75e1
variant carriers: 46

African
type: Population
allele count: 44
allele frequency: 4.299394176275161e-3
allele num: 10234
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.74246384387524e-4
allele num: 11478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64204
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9640
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.196e1

FS
type: SiteQuality
SIO_000300: 1.262e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.846e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQ
type: SiteQuality
SIO_000300: 5.946e1

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

DP
type: SiteQuality
SIO_000300: 1.891208e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.67e-1