8-1842572-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842572
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842572
    reference: chr 8
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1349C>T
  hgvsp: ENSP00000431012.1:p.Pro450Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1160C>T
  hgvsp: ENSP00000427909.1:p.Pro387Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1349C>T
  hgvsp: ENSP00000262112.6:p.Pro450Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.998C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1349C>T
  hgvsp: ENSP00000381571.1:p.Pro450Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1232C>T
  hgvsp: ENSP00000381568.1:p.Pro411Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1274C>T
  hgvsp: ENSP00000340297.3:p.Pro425Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.970C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.293C>T
  hgvsp: ENSP00000427768.1:p.Pro98Leu
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2384
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro425Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

8-1842573-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842573
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842573
    reference: chr 8
allele count: 39
allele frequency: 3.217556307235376e-4
allele num: 121210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1350G>A
  hgvsp: ENST00000262112.6:c.1350G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1275G>A
  hgvsp: ENST00000349830.3:c.1275G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1161G>A
  hgvsp: ENST00000520359.1:c.1161G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.294G>A
  hgvsp: ENST00000522435.1:c.294G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1233G>A
  hgvsp: ENST00000398560.1:c.1233G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.971G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1350G>A
  hgvsp: ENST00000398564.1:c.1350G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1350G>A
  hgvsp: ENST00000518288.1:c.1350G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.999G>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15898
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 38353
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro425Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

8-1842576-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842576
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842576
    reference: chr 8
allele count: 1
allele frequency: 8.247966876165026e-6
allele num: 121242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1164G>A
  hgvsp: ENST00000520359.1:c.1164G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.974G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1278G>A
  hgvsp: ENST00000349830.3:c.1278G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1353G>A
  hgvsp: ENST00000518288.1:c.1353G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1353G>A
  hgvsp: ENST00000262112.6:c.1353G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1353G>A
  hgvsp: ENST00000398564.1:c.1353G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1236G>A
  hgvsp: ENST00000398560.1:c.1236G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.297G>A
  hgvsp: ENST00000522435.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1002G>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu426Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-1842578-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842578
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842578
    reference: chr 8
allele count: 1
allele frequency: 8.247422680412371e-6
allele num: 121250
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1004C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1238C>T
  hgvsp: ENSP00000381568.1:p.Ser413Phe
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1166C>T
  hgvsp: ENSP00000427909.1:p.Ser389Phe
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1355C>T
  hgvsp: ENSP00000381571.1:p.Ser452Phe
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1355C>T
  hgvsp: ENSP00000431012.1:p.Ser452Phe
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.299C>T
  hgvsp: ENSP00000427768.1:p.Ser100Phe
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1280C>T
  hgvsp: ENSP00000340297.3:p.Ser427Phe
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.976C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1355C>T
  hgvsp: ENSP00000262112.6:p.Ser452Phe
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7067
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6417
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser427Phe
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff

8-1842581-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842581
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842581
    reference: chr 8
allele count: 7
allele frequency: 5.772434153018983e-5
allele num: 121266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1358A>T
  hgvsp: ENSP00000262112.6:p.Glu453Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1007A>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1283A>T
  hgvsp: ENSP00000340297.3:p.Glu428Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1241A>T
  hgvsp: ENSP00000381568.1:p.Glu414Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1358A>T
  hgvsp: ENSP00000381571.1:p.Glu453Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1358A>T
  hgvsp: ENSP00000431012.1:p.Glu453Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.979A>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1169A>T
  hgvsp: ENSP00000427909.1:p.Glu390Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.302A>T
  hgvsp: ENSP00000427768.1:p.Glu101Val
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6076
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu428Val
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

8-1842582-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842582
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842582
    reference: chr 8
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1284G>C
  hgvsp: ENSP00000340297.3:p.Glu428Asp
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1359G>C
  hgvsp: ENSP00000431012.1:p.Glu453Asp
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.303G>C
  hgvsp: ENSP00000427768.1:p.Glu101Asp
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1008G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1359G>C
  hgvsp: ENSP00000262112.6:p.Glu453Asp
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1170G>C
  hgvsp: ENSP00000427909.1:p.Glu390Asp
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1359G>C
  hgvsp: ENSP00000381571.1:p.Glu453Asp
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.980G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1242G>C
  hgvsp: ENSP00000381568.1:p.Glu414Asp
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30500
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15978
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu428Asp
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

8-1842583-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842583
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842583
    reference: chr 8
allele count: 2
allele frequency: 1.649049323065253e-5
allele num: 121282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1171A>T
  hgvsp: ENSP00000427909.1:p.Met391Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1360A>T
  hgvsp: ENSP00000381571.1:p.Met454Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1360A>T
  hgvsp: ENSP00000262112.6:p.Met454Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1360A>T
  hgvsp: ENSP00000431012.1:p.Met454Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1243A>T
  hgvsp: ENSP00000381568.1:p.Met415Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.981A>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1009A>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.304A>T
  hgvsp: ENSP00000427768.1:p.Met102Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1285A>T
  hgvsp: ENSP00000340297.3:p.Met429Leu
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1006
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Met429Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-1842601-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842601
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842601
    reference: chr 8
allele count: 1
allele frequency: 8.243071698237632e-6
allele num: 121314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1027A>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.322A>C
  hgvsp: ENSP00000427768.1:p.Ser108Arg
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1303A>C
  hgvsp: ENSP00000340297.3:p.Ser435Arg
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1378A>C
  hgvsp: ENSP00000262112.6:p.Ser460Arg
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1378A>C
  hgvsp: ENSP00000431012.1:p.Ser460Arg
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1189A>C
  hgvsp: ENSP00000427909.1:p.Ser397Arg
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1378A>C
  hgvsp: ENSP00000381571.1:p.Ser460Arg
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.999A>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1261A>C
  hgvsp: ENSP00000381568.1:p.Ser421Arg
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2364
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser435Arg
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum

8-1842605-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842605
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842605
    reference: chr 8
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1265A>G
  hgvsp: ENSP00000381568.1:p.Glu422Gly
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1382A>G
  hgvsp: ENSP00000431012.1:p.Glu461Gly
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1031A>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1382A>G
  hgvsp: ENSP00000262112.6:p.Glu461Gly
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1193A>G
  hgvsp: ENSP00000427909.1:p.Glu398Gly
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1382A>G
  hgvsp: ENSP00000381571.1:p.Glu461Gly
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.326A>G
  hgvsp: ENSP00000427768.1:p.Glu109Gly
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1003A>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1307A>G
  hgvsp: ENSP00000340297.3:p.Glu436Gly
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2748
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu436Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP

8-1842613-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842613
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842613
    reference: chr 8
allele count: 39
allele frequency: 3.214638971315529e-4
allele num: 121320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1390C>G
  hgvsp: ENSP00000262112.6:p.Leu464Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1390C>G
  hgvsp: ENSP00000381571.1:p.Leu464Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1390C>G
  hgvsp: ENSP00000431012.1:p.Leu464Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1011C>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1273C>G
  hgvsp: ENSP00000381568.1:p.Leu425Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1315C>G
  hgvsp: ENSP00000340297.3:p.Leu439Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1039C>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1201C>G
  hgvsp: ENSP00000427909.1:p.Leu401Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.334C>G
  hgvsp: ENSP00000427768.1:p.Leu112Val
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30253
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16100
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 6115
  bin: 3.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1007
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2364
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu439Val
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

8-1842620-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842620
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842620
    reference: chr 8
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1046C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1018C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1208C>T
  hgvsp: ENSP00000427909.1:p.Thr403Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1322C>T
  hgvsp: ENSP00000340297.3:p.Thr441Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1397C>T
  hgvsp: ENSP00000262112.6:p.Thr466Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1397C>T
  hgvsp: ENSP00000381571.1:p.Thr466Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.341C>T
  hgvsp: ENSP00000427768.1:p.Thr114Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1397C>T
  hgvsp: ENSP00000431012.1:p.Thr466Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1280C>T
  hgvsp: ENSP00000381568.1:p.Thr427Met
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16115
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr441Met
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

8-1842621-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842621
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842621
    reference: chr 8
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1398G>A
  hgvsp: ENST00000518288.1:c.1398G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1323G>A
  hgvsp: ENST00000349830.3:c.1323G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1019G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1398G>A
  hgvsp: ENST00000398564.1:c.1398G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1398G>A
  hgvsp: ENST00000262112.6:c.1398G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.342G>A
  hgvsp: ENST00000522435.1:c.342G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1047G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1209G>A
  hgvsp: ENST00000520359.1:c.1209G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1281G>A
  hgvsp: ENST00000398560.1:c.1281G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr441Thr
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: G
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/8-1842627-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842627
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842627
    reference: chr 8
allele count: 2
allele frequency: 1.648451280022419e-5
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1215C>A
  hgvsp: ENSP00000427909.1:p.Phe405Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1404C>A
  hgvsp: ENSP00000431012.1:p.Phe468Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1404C>A
  hgvsp: ENSP00000381571.1:p.Phe468Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1287C>A
  hgvsp: ENSP00000381568.1:p.Phe429Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1329C>A
  hgvsp: ENSP00000340297.3:p.Phe443Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1404C>A
  hgvsp: ENSP00000262112.6:p.Phe468Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1025C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.348C>A
  hgvsp: ENSP00000427768.1:p.Phe116Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1053C>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16178
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30133
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1005
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Phe443Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD

8-1842629-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842629
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842629
    reference: chr 8
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1406A>G
  hgvsp: ENSP00000262112.6:p.Tyr469Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.350A>G
  hgvsp: ENSP00000427768.1:p.Tyr117Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1331A>G
  hgvsp: ENSP00000340297.3:p.Tyr444Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1027A>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1406A>G
  hgvsp: ENSP00000381571.1:p.Tyr469Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1289A>G
  hgvsp: ENSP00000381568.1:p.Tyr430Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1217A>G
  hgvsp: ENSP00000427909.1:p.Tyr406Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1055A>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1406A>G
  hgvsp: ENSP00000431012.1:p.Tyr469Cys
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38157
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Tyr444Cys
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

8-1842645-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842645
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842645
    reference: chr 8
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1347C>T
  hgvsp: ENST00000349830.3:c.1347C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1043C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1422C>T
  hgvsp: ENST00000262112.6:c.1422C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1071C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1422C>T
  hgvsp: ENST00000518288.1:c.1422C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.366C>T
  hgvsp: ENST00000522435.1:c.366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1233C>T
  hgvsp: ENST00000520359.1:c.1233C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1422C>T
  hgvsp: ENST00000398564.1:c.1422C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1305C>T
  hgvsp: ENST00000398560.1:c.1305C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6423
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile449Ile
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/8-1842646-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842646
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842646
    reference: chr 8
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1072C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1306C>A
  hgvsp: ENSP00000381568.1:p.Leu436Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1234C>A
  hgvsp: ENSP00000427909.1:p.Leu412Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1423C>A
  hgvsp: ENSP00000381571.1:p.Leu475Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1044C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1423C>A
  hgvsp: ENSP00000431012.1:p.Leu475Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1348C>A
  hgvsp: ENSP00000340297.3:p.Leu450Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.367C>A
  hgvsp: ENSP00000427768.1:p.Leu123Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1423C>A
  hgvsp: ENSP00000262112.6:p.Leu475Met
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29933
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7100
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu450Met
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

8-1842648-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842648
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842648
    reference: chr 8
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1308G>C
  hgvsp: ENST00000398560.1:c.1308G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1046G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1350G>C
  hgvsp: ENST00000349830.3:c.1350G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1236G>C
  hgvsp: ENST00000520359.1:c.1236G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1425G>C
  hgvsp: ENST00000398564.1:c.1425G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.369G>C
  hgvsp: ENST00000522435.1:c.369G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1425G>C
  hgvsp: ENST00000518288.1:c.1425G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1425G>C
  hgvsp: ENST00000262112.6:c.1425G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1074G>C
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7101
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2743
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu450Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-1842654-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842654
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842654
    reference: chr 8
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1431C>T
  hgvsp: ENST00000398564.1:c.1431C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1431C>T
  hgvsp: ENST00000518288.1:c.1431C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1431C>T
  hgvsp: ENST00000262112.6:c.1431C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.375C>T
  hgvsp: ENST00000522435.1:c.375C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1314C>T
  hgvsp: ENST00000398560.1:c.1314C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1052C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1356C>T
  hgvsp: ENST00000349830.3:c.1356C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1080C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1242C>T
  hgvsp: ENST00000520359.1:c.1242C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6158
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1775
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys452Cys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

8-1842660-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842660
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842660
    reference: chr 8
allele count: 6
allele frequency: 4.945679948564928e-5
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1437G>A
  hgvsp: ENST00000518288.1:c.1437G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1086G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1437G>A
  hgvsp: ENST00000398564.1:c.1437G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1437G>A
  hgvsp: ENST00000262112.6:c.1437G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1362G>A
  hgvsp: ENST00000349830.3:c.1362G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1248G>A
  hgvsp: ENST00000520359.1:c.1248G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.381G>A
  hgvsp: ENST00000522435.1:c.381G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1320G>A
  hgvsp: ENST00000398560.1:c.1320G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1058G>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2365
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7105
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser454Ser
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

8-1842660-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842660
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842660
    reference: chr 8
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1320G>C
  hgvsp: ENST00000398560.1:c.1320G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1437G>C
  hgvsp: ENST00000398564.1:c.1437G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1362G>C
  hgvsp: ENST00000349830.3:c.1362G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1437G>C
  hgvsp: ENST00000262112.6:c.1437G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1437G>C
  hgvsp: ENST00000518288.1:c.1437G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.381G>C
  hgvsp: ENST00000522435.1:c.381G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1248G>C
  hgvsp: ENST00000520359.1:c.1248G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1058G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1086G>C
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2741
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser454Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP

8-1842661-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842661
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842661
    reference: chr 8
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1087C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1438C>T
  hgvsp: ENST00000398564.1:c.1438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1438C>T
  hgvsp: ENST00000262112.6:c.1438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1363C>T
  hgvsp: ENST00000349830.3:c.1363C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1059C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1321C>T
  hgvsp: ENST00000398560.1:c.1321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1438C>T
  hgvsp: ENST00000518288.1:c.1438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.382C>T
  hgvsp: ENST00000522435.1:c.382C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1249C>T
  hgvsp: ENST00000520359.1:c.1249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2370
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu455Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

8-1842663-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842663
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842663
    reference: chr 8
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1323A>G
  hgvsp: ENST00000398560.1:c.1323A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1440A>G
  hgvsp: ENST00000262112.6:c.1440A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1251A>G
  hgvsp: ENST00000520359.1:c.1251A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1440A>G
  hgvsp: ENST00000398564.1:c.1440A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1365A>G
  hgvsp: ENST00000349830.3:c.1365A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1440A>G
  hgvsp: ENST00000518288.1:c.1440A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.384A>G
  hgvsp: ENST00000522435.1:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1061A>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1089A>G
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6179
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38143
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 742
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu455Leu
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

8-1842663-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842663
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842663
    reference: chr 8
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1251A>T
  hgvsp: ENST00000520359.1:c.1251A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1440A>T
  hgvsp: ENST00000398564.1:c.1440A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1089A>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1365A>T
  hgvsp: ENST00000349830.3:c.1365A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1323A>T
  hgvsp: ENST00000398560.1:c.1323A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1440A>T
  hgvsp: ENST00000262112.6:c.1440A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1061A>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.384A>T
  hgvsp: ENST00000522435.1:c.384A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1440A>T
  hgvsp: ENST00000518288.1:c.1440A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38143
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu455Leu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/8-1842668-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842668
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842668
    reference: chr 8
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1445A>C
  hgvsp: ENSP00000431012.1:p.Gln482Pro
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1328A>C
  hgvsp: ENSP00000381568.1:p.Gln443Pro
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1094A>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.389A>C
  hgvsp: ENSP00000427768.1:p.Gln130Pro
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1445A>C
  hgvsp: ENSP00000262112.6:p.Gln482Pro
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1445A>C
  hgvsp: ENSP00000381571.1:p.Gln482Pro
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1370A>C
  hgvsp: ENSP00000340297.3:p.Gln457Pro
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1256A>C
  hgvsp: ENSP00000427909.1:p.Gln419Pro
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1066A>C
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6426
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gln457Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-1842672-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842672
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842672
    reference: chr 8
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1374C>A
  hgvsp: ENST00000349830.3:c.1374C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1070C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1449C>A
  hgvsp: ENST00000398564.1:c.1449C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.393C>A
  hgvsp: ENST00000522435.1:c.393C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1449C>A
  hgvsp: ENST00000262112.6:c.1449C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1098C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1260C>A
  hgvsp: ENST00000520359.1:c.1260C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1449C>A
  hgvsp: ENST00000518288.1:c.1449C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1332C>A
  hgvsp: ENST00000398560.1:c.1332C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6427
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile458Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

8-1842672-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842672
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842672
    reference: chr 8
allele count: 2
allele frequency: 1.648424106554134e-5
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1260C>T
  hgvsp: ENST00000520359.1:c.1260C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1449C>T
  hgvsp: ENST00000262112.6:c.1449C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1374C>T
  hgvsp: ENST00000349830.3:c.1374C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1449C>T
  hgvsp: ENST00000518288.1:c.1449C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1332C>T
  hgvsp: ENST00000398560.1:c.1332C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.393C>T
  hgvsp: ENST00000522435.1:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1449C>T
  hgvsp: ENST00000398564.1:c.1449C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1070C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1098C>T
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile458Ile
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

8-1842674-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842674
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842674
    reference: chr 8
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1262C>T
  hgvsp: ENSP00000427909.1:p.Ala421Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1451C>T
  hgvsp: ENSP00000262112.6:p.Ala484Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1451C>T
  hgvsp: ENSP00000431012.1:p.Ala484Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1334C>T
  hgvsp: ENSP00000381568.1:p.Ala445Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1451C>T
  hgvsp: ENSP00000381571.1:p.Ala484Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.395C>T
  hgvsp: ENSP00000427768.1:p.Ala132Val
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1100C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1072C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1376C>T
  hgvsp: ENSP00000340297.3:p.Ala459Val
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala459Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

8-1842675-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842675
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842675
    reference: chr 8
allele count: 2
allele frequency: 1.648478454386601e-5
allele num: 121324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1335G>A
  hgvsp: ENST00000398560.1:c.1335G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1452G>A
  hgvsp: ENST00000398564.1:c.1452G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.396G>A
  hgvsp: ENST00000522435.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1452G>A
  hgvsp: ENST00000518288.1:c.1452G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1452G>A
  hgvsp: ENST00000262112.6:c.1452G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1263G>A
  hgvsp: ENST00000520359.1:c.1263G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1377G>A
  hgvsp: ENST00000349830.3:c.1377G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1073G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1101G>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16520
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38140
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6427
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Ala459Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

8-1842685-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842685
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842685
    reference: chr 8
allele count: 2
allele frequency: 1.648451280022419e-5
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.406C>T
  hgvsp: ENSP00000427768.1:p.Arg136Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1462C>T
  hgvsp: ENSP00000262112.6:p.Arg488Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1111C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1462C>T
  hgvsp: ENSP00000381571.1:p.Arg488Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1387C>T
  hgvsp: ENSP00000340297.3:p.Arg463Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1273C>T
  hgvsp: ENSP00000427909.1:p.Arg425Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1083C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1462C>T
  hgvsp: ENSP00000431012.1:p.Arg488Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1345C>T
  hgvsp: ENSP00000381568.1:p.Arg449Cys
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29598
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1006
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg463Cys
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

8-1842688-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842688
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842688
    reference: chr 8
allele count: 5
allele frequency: 4.121060266385336e-5
allele num: 121328
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1348G>A
  hgvsp: ENSP00000381568.1:p.Val450Ile
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1465G>A
  hgvsp: ENSP00000431012.1:p.Val489Ile
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1465G>A
  hgvsp: ENSP00000262112.6:p.Val489Ile
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1114G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1086G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1465G>A
  hgvsp: ENSP00000381571.1:p.Val489Ile
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.409G>A
  hgvsp: ENSP00000427768.1:p.Val137Ile
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1276G>A
  hgvsp: ENSP00000427909.1:p.Val426Ile
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1390G>A
  hgvsp: ENSP00000340297.3:p.Val464Ile
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29588
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7148
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1006
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val464Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

8-1842691-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842691
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842691
    reference: chr 8
allele count: 8
allele frequency: 6.593805120089676e-5
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1279T>A
  hgvsp: ENSP00000427909.1:p.Ser427Thr
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1468T>A
  hgvsp: ENSP00000431012.1:p.Ser490Thr
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1117T>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1351T>A
  hgvsp: ENSP00000381568.1:p.Ser451Thr
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1393T>A
  hgvsp: ENSP00000340297.3:p.Ser465Thr
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1468T>A
  hgvsp: ENSP00000381571.1:p.Ser490Thr
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1089T>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1468T>A
  hgvsp: ENSP00000262112.6:p.Ser490Thr
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.412T>A
  hgvsp: ENSP00000427768.1:p.Ser138Thr
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser465Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP

8-1842693-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842693
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842693
    reference: chr 8
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1470C>T
  hgvsp: ENST00000518288.1:c.1470C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1395C>T
  hgvsp: ENST00000349830.3:c.1395C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1353C>T
  hgvsp: ENST00000398560.1:c.1353C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1281C>T
  hgvsp: ENST00000520359.1:c.1281C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.414C>T
  hgvsp: ENST00000522435.1:c.414C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1470C>T
  hgvsp: ENST00000398564.1:c.1470C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1119C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1091C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1470C>T
  hgvsp: ENST00000262112.6:c.1470C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser465Ser
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

8-1842694-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842694
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842694
    reference: chr 8
allele count: 25
allele frequency: 2.060666007253544e-4
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.415G>A
  hgvsp: ENSP00000427768.1:p.Glu139Lys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1282G>A
  hgvsp: ENSP00000427909.1:p.Glu428Lys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1471G>A
  hgvsp: ENSP00000262112.6:p.Glu491Lys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1396G>A
  hgvsp: ENSP00000340297.3:p.Glu466Lys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1471G>A
  hgvsp: ENSP00000381571.1:p.Glu491Lys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1092G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1354G>A
  hgvsp: ENSP00000381568.1:p.Glu452Lys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1471G>A
  hgvsp: ENSP00000431012.1:p.Glu491Lys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1120G>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 16649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2366
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu466Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

8-1842697-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842697
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842697
    reference: chr 8
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1474T>C
  hgvsp: ENSP00000431012.1:p.Trp492Arg
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1285T>C
  hgvsp: ENSP00000427909.1:p.Trp429Arg
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1357T>C
  hgvsp: ENSP00000381568.1:p.Trp453Arg
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1123T>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1095T>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1474T>C
  hgvsp: ENSP00000381571.1:p.Trp492Arg
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1399T>C
  hgvsp: ENSP00000340297.3:p.Trp467Arg
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.418T>C
  hgvsp: ENSP00000427768.1:p.Trp140Arg
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1474T>C
  hgvsp: ENSP00000262112.6:p.Trp492Arg
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6206
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16663
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Trp467Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ

8-1842704-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842704
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842704
    reference: chr 8
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1292C>G
  hgvsp: ENSP00000427909.1:p.Ser431Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1406C>G
  hgvsp: ENSP00000340297.3:p.Ser469Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.425C>G
  hgvsp: ENSP00000427768.1:p.Ser142Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1364C>G
  hgvsp: ENSP00000381568.1:p.Ser455Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1481C>G
  hgvsp: ENSP00000381571.1:p.Ser494Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1481C>G
  hgvsp: ENSP00000431012.1:p.Ser494Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1481C>G
  hgvsp: ENSP00000262112.6:p.Ser494Cys
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1130C>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1102C>G
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29542
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16693
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser469Cys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-1842705-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842705
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842705
    reference: chr 8
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1482C>A
  hgvsp: ENST00000262112.6:c.1482C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.426C>A
  hgvsp: ENST00000522435.1:c.426C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1365C>A
  hgvsp: ENST00000398560.1:c.1365C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1293C>A
  hgvsp: ENST00000520359.1:c.1293C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1482C>A
  hgvsp: ENST00000398564.1:c.1482C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1482C>A
  hgvsp: ENST00000518288.1:c.1482C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1103C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1407C>A
  hgvsp: ENST00000349830.3:c.1407C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1131C>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 746
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2367
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser469Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

8-1842705-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842705
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842705
    reference: chr 8
allele count: 6
allele frequency: 4.946658532161525e-5
allele num: 121294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1482C>T
  hgvsp: ENST00000262112.6:c.1482C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1482C>T
  hgvsp: ENST00000398564.1:c.1482C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.426C>T
  hgvsp: ENST00000522435.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1365C>T
  hgvsp: ENST00000398560.1:c.1365C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1293C>T
  hgvsp: ENST00000520359.1:c.1293C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1131C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1482C>T
  hgvsp: ENST00000518288.1:c.1482C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1103C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1407C>T
  hgvsp: ENST00000349830.3:c.1407C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16694
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7148
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser469Ser
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

8-1842706-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842706
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842706
    reference: chr 8
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1483G>A
  hgvsp: ENSP00000431012.1:p.Val495Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.427G>A
  hgvsp: ENSP00000427768.1:p.Val143Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1483G>A
  hgvsp: ENSP00000381571.1:p.Val495Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1132G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1483G>A
  hgvsp: ENSP00000262112.6:p.Val495Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1294G>A
  hgvsp: ENSP00000427909.1:p.Val432Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1408G>A
  hgvsp: ENSP00000340297.3:p.Val470Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1366G>A
  hgvsp: ENSP00000381568.1:p.Val456Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1104G>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val470Met
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

8-1842706-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842706
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842706
    reference: chr 8
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1408G>T
  hgvsp: ENSP00000340297.3:p.Val470Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1483G>T
  hgvsp: ENSP00000381571.1:p.Val495Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1483G>T
  hgvsp: ENSP00000431012.1:p.Val495Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1132G>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1483G>T
  hgvsp: ENSP00000262112.6:p.Val495Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1294G>T
  hgvsp: ENSP00000427909.1:p.Val432Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1104G>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.427G>T
  hgvsp: ENSP00000427768.1:p.Val143Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1366G>T
  hgvsp: ENSP00000381568.1:p.Val456Leu
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16697
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val470Leu
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

8-1842716-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842716
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842716
    reference: chr 8
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1304T>C
  hgvsp: ENSP00000427909.1:p.Ile435Thr
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1418T>C
  hgvsp: ENSP00000340297.3:p.Ile473Thr
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1493T>C
  hgvsp: ENSP00000262112.6:p.Ile498Thr
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.437T>C
  hgvsp: ENSP00000427768.1:p.Ile146Thr
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1376T>C
  hgvsp: ENSP00000381568.1:p.Ile459Thr
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1493T>C
  hgvsp: ENSP00000381571.1:p.Ile498Thr
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1114T>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1493T>C
  hgvsp: ENSP00000431012.1:p.Ile498Thr
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1142T>C
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1195
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1775
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile473Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

8-1842720-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842720
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842720
    reference: chr 8
allele count: 2
allele frequency: 1.649620587264929e-5
allele num: 121240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1497C>T
  hgvsp: ENST00000518288.1:c.1497C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1308C>T
  hgvsp: ENST00000520359.1:c.1308C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1422C>T
  hgvsp: ENST00000349830.3:c.1422C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1497C>T
  hgvsp: ENST00000398564.1:c.1497C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1118C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.441C>T
  hgvsp: ENST00000522435.1:c.441C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1497C>T
  hgvsp: ENST00000262112.6:c.1497C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1146C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1380C>T
  hgvsp: ENST00000398560.1:c.1380C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16707
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29427
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7141
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly474Gly
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-1842723-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842723
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842723
    reference: chr 8
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1500T>A
  hgvsp: ENSP00000262112.6:p.Asp500Glu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1121T>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1311T>A
  hgvsp: ENSP00000427909.1:p.Asp437Glu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.444T>A
  hgvsp: ENSP00000427768.1:p.Asp148Glu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1383T>A
  hgvsp: ENSP00000381568.1:p.Asp461Glu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1425T>A
  hgvsp: ENSP00000340297.3:p.Asp475Glu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1500T>A
  hgvsp: ENSP00000431012.1:p.Asp500Glu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1500T>A
  hgvsp: ENSP00000381571.1:p.Asp500Glu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1149T>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2359
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp475Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

8-1842723-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842723
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842723
    reference: chr 8
allele count: 1
allele frequency: 8.24905548314718e-6
allele num: 121226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1311T>C
  hgvsp: ENST00000520359.1:c.1311T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1500T>C
  hgvsp: ENST00000518288.1:c.1500T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1425T>C
  hgvsp: ENST00000349830.3:c.1425T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1500T>C
  hgvsp: ENST00000398564.1:c.1500T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1500T>C
  hgvsp: ENST00000262112.6:c.1500T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1383T>C
  hgvsp: ENST00000398560.1:c.1383T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.444T>C
  hgvsp: ENST00000522435.1:c.444T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1121T>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1149T>C
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1544
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp475Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

8-1842726-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842726
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842726
    reference: chr 8
allele count: 5
allele frequency: 4.126365827088766e-5
allele num: 121172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1503C>T
  hgvsp: ENST00000262112.6:c.1503C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1386C>T
  hgvsp: ENST00000398560.1:c.1386C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1428C>T
  hgvsp: ENST00000349830.3:c.1428C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1152C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1124C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1314C>T
  hgvsp: ENST00000520359.1:c.1314C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1503C>T
  hgvsp: ENST00000398564.1:c.1503C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1503C>T
  hgvsp: ENST00000518288.1:c.1503C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.447C>T
  hgvsp: ENST00000522435.1:c.447C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6215
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16711
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Val476Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

8-1842729-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842729
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842729
    reference: chr 8
allele count: 680
allele frequency: 5.612228054537652e-3
allele num: 121164
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1127C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1317C>T
  hgvsp: ENST00000520359.1:c.1317C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1506C>T
  hgvsp: ENST00000518288.1:c.1506C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1389C>T
  hgvsp: ENST00000398560.1:c.1389C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.450C>T
  hgvsp: ENST00000522435.1:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1155C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1506C>T
  hgvsp: ENST00000398564.1:c.1506C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1506C>T
  hgvsp: ENST00000262112.6:c.1506C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1431C>T
  hgvsp: ENST00000349830.3:c.1431C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 6.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16552
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 28947
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6133
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 3.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 4.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 4.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.75e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 8.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 5.25e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 5.75e1
  variant carriers: 69
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 1
hgvs: p.Phe477Phe
num of homozygotes: 22
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

8-1842730-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842730
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842730
    reference: chr 8
allele count: 3
allele frequency: 2.476269087907552e-5
allele num: 121150
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1507G>A
  hgvsp: ENSP00000381571.1:p.Val503Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1128G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1318G>A
  hgvsp: ENSP00000427909.1:p.Val440Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1507G>A
  hgvsp: ENSP00000431012.1:p.Val503Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.451G>A
  hgvsp: ENSP00000427768.1:p.Val151Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1507G>A
  hgvsp: ENSP00000262112.6:p.Val503Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1156G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1390G>A
  hgvsp: ENSP00000381568.1:p.Val464Met
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1432G>A
  hgvsp: ENSP00000340297.3:p.Val478Met
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28990
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16784
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7057
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val478Met
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum

8-1842737-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842737
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842737
    reference: chr 8
allele count: 6
allele frequency: 4.9572028156912e-5
allele num: 121036
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1514C>T
  hgvsp: ENSP00000431012.1:p.Ser505Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.458C>T
  hgvsp: ENSP00000427768.1:p.Ser153Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1514C>T
  hgvsp: ENSP00000262112.6:p.Ser505Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1135C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1325C>T
  hgvsp: ENSP00000427909.1:p.Ser442Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1397C>T
  hgvsp: ENSP00000381568.1:p.Ser466Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1514C>T
  hgvsp: ENSP00000381571.1:p.Ser505Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1439C>T
  hgvsp: ENSP00000340297.3:p.Ser480Leu
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1163C>T
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser480Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum

8-1842739-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842739
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842739
    reference: chr 8
allele count: 2
allele frequency: 1.653083827880912e-5
allele num: 120986
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+1G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+1G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+1G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+1G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+1G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+1G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+1G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+1G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+1G>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16750
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2321
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37712
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6449
  bin: 9.75e1
  variant carriers: 2
hgvs: c.1440+1G>A
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

8-1842748-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842748
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842748
    reference: chr 8
allele count: 317
allele frequency: 2.62521531734464e-3
allele num: 120752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+10C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+10C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+10C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+10C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+10C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+10C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+10C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+10C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+10C>T
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27694
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 16471
  bin: 2.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 4.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 3.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 5.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 5.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 4.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 6241
  bin: 3.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 6.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1726
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 2
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

8-1842751-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842751
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842751
    reference: chr 8
allele count: 1
allele frequency: 8.284592315212168e-6
allele num: 120706
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+13G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+13G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+13G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+13G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+13G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+13G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+13G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+13G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+13G>C
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 936
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2287
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

8-1842756-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842756
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842756
    reference: chr 8
allele count: 1
allele frequency: 8.29476268683953e-6
allele num: 120558
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+18C>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+18C>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+18C>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+18C>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+18C>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+18C>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+18C>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+18C>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+18C>G
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6828
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/8-1842756-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842756
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842756
    reference: chr 8
allele count: 3
allele frequency: 2.488428806051859e-5
allele num: 120558
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+18C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+18C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+18C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+18C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+18C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+18C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+18C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+18C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+18C>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6223
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6828
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35270
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum

8-1842756-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842756
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842756
    reference: chr 8
allele count: 1
allele frequency: 8.29476268683953e-6
allele num: 120558
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+18C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+18C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+18C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+18C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+18C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+18C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+18C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+18C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+18C>T
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6223
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26775
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35270
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1290
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2279
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2646
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

8-1842760-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842760
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842760
    reference: chr 8
allele count: 1
allele frequency: 8.29985724245543e-6
allele num: 120484
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+22G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+22G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+22G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+22G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+22G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+22G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+22G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+22G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+22G>C
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2244
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2619
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34168
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1651
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-1842760-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842760
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842760
    reference: chr 8
allele count: 2
allele frequency: 1.659971448491086e-5
allele num: 120484
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+22G>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+22G>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+22G>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+22G>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+22G>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+22G>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+22G>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+22G>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+22G>T
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1552
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16129
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25696
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 696
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum

http://identifiers.org/exac.variant/8-1842766-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842766
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842766
    reference: chr 8
allele count: 1
allele frequency: 8.310203267571925e-6
allele num: 120334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+28C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+28C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+28C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+28C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+28C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+28C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+28C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+28C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+28C>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24236
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1709
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2587
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2203
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32282
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

8-1842768-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842768
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842768
    reference: chr 8
allele count: 1
allele frequency: 8.308822307526131e-6
allele num: 120354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+30T>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+30T>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+30T>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+30T>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+30T>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+30T>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+30T>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+30T>G
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+30T>G
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23637
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3642
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2575
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2192
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6436
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

8-1842772-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842772
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842772
    reference: chr 8
allele count: 2
allele frequency: 1.663561352142667e-5
allele num: 120224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+34G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+34G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+34G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+34G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+34G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+34G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+34G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+34G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+34G>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5899
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2787
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27462
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2116
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1520
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-1842773-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842773
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842773
    reference: chr 8
allele count: 1
allele frequency: 8.320713584396998e-6
allele num: 120182
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+35C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+35C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+35C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+35C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+35C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+35C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+35C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+35C>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+35C>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14521
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1698
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1518
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1045
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2570
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2120
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

8-1842775-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842775
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842775
    reference: chr 8
allele count: 3
allele frequency: 2.49820961644155e-5
allele num: 120086
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+37C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+37C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+37C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+37C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+37C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+37C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+37C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+37C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+37C>T
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8727
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5731
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13553
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4338
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 895
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3361
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1669
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1693
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum

8-1842776-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842776
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842776
    reference: chr 8
allele count: 1
allele frequency: 8.328891257995735e-6
allele num: 120064
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+38T>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+38T>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+38T>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+38T>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+38T>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+38T>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+38T>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+38T>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+38T>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8723
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13580
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3532
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1669
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3361
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

8-1842780-T-TCTGTTTTCCATGAATTG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842780
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842797
    reference: chr 8
allele count: 1
allele frequency: 8.338753523123364e-6
allele num: 119922
alternate allele: TCTGTTTTCCATGAATTG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5510
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10000
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5469
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3675
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1684
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2731
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD

8-1842782-C-CAAATTGGAAGTACAATGATCACTAGCTGGACTGTGTTTAGAATGAGGG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842782
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842830
    reference: chr 8
allele count: 1
allele frequency: 8.361343835181191e-6
allele num: 119598
alternate allele: CAAATTGGAAGTACAATGATCACTAGCTGGACTGTGTTTAGAATGAGGG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20096
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9993
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3857
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1894
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5239
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6428
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1709
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2001
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-1842782-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842782
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842782
    reference: chr 8
allele count: 1
allele frequency: 8.361343835181191e-6
allele num: 119598
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+44C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+44C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+44C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+44C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+44C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+44C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+44C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+44C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+44C>T
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 2395
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9993
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20096
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11976
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19395
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3573
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6428
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5239
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS

8-1842784-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842784
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842784
    reference: chr 8
allele count: 1
allele frequency: 8.36638053645232e-6
allele num: 119526
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+46C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+46C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+46C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+46C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+46C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+46C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+46C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+46C>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+46C>T
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20479
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9983
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11688
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1680
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17770
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1922
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2313
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

8-1842787-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1842787
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1842787
    reference: chr 8
allele count: 1
allele frequency: 8.392077878482712e-6
allele num: 119160
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.459+49G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1515+49G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1440+49G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1398+49G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1164+49G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1515+49G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1326+49G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1515+49G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1136+49G>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11705
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9932
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5032
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4792
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2434
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1673
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP

8-1844449-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1844449
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1844449
    reference: chr 8
allele count: 4
allele frequency: 3.312519668085529e-5
allele num: 120754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1137-50G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1399-50G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1327-50G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1441-50G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1516-50G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1516-50G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.460-50G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1165-50G>A
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1516-50G>A
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8814
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3905
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4282
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4961
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2365
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-1844450-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1844450
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1844450
    reference: chr 8
allele count: 2
allele frequency: 1.656259834042764e-5
allele num: 120754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1516-49G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1137-49G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.460-49G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1165-49G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1516-49G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1399-49G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1441-49G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1516-49G>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1327-49G>C
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4282
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4962
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8812
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3905
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2274
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42004
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2356
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

8-1844453-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1844453
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1844453
    reference: chr 8
allele count: 2
allele frequency: 1.656067832538421e-5
allele num: 120768
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1137-46T>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1516-46T>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1441-46T>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.460-46T>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1516-46T>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1165-46T>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1516-46T>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1327-46T>C
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1399-46T>C
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4964
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3905
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4281
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8812
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4326
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2356
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2365
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1758
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

8-1844454-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 1844454
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 1844454
    reference: chr 8
allele count: 55
allele frequency: 4.554261961148005e-4
allele num: 120766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000523711
  gene symbol: ARHGEF10
  hgvsc: ENST00000523711.1:n.1165-45A>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl transcript: ENST00000520972
  gene symbol: ARHGEF10
  hgvsc: ENST00000520972.1:n.1137-45A>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000340297
  ensembl transcript: ENST00000349830
  gene symbol: ARHGEF10
  hgvsc: ENST00000349830.3:c.1441-45A>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381571
  ensembl transcript: ENST00000398564
  gene symbol: ARHGEF10
  hgvsc: ENST00000398564.1:c.1516-45A>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000262112
  ensembl transcript: ENST00000262112
  gene symbol: ARHGEF10
  hgvsc: ENST00000262112.6:c.1516-45A>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000381568
  ensembl transcript: ENST00000398560
  gene symbol: ARHGEF10
  hgvsc: ENST00000398560.1:c.1399-45A>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427768
  ensembl transcript: ENST00000522435
  gene symbol: ARHGEF10
  hgvsc: ENST00000522435.1:c.460-45A>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000431012
  ensembl transcript: ENST00000518288
  gene symbol: ARHGEF10
  hgvsc: ENST00000518288.1:c.1516-45A>T
  variant of: http://identifiers.org/hgnc/14103
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000104728
  ensembl protein: ENSP00000427909
  ensembl transcript: ENST00000520359
  gene symbol: ARHGEF10
  hgvsc: ENST00000520359.1:c.1327-45A>T
  variant of: http://identifiers.org/hgnc/14103
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4960
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1871
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4283
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4543
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8815
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 1006
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2353
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7050
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1777
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2748
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38370
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6413
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 740
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500690317546071e-5
allele num: 66636
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

FS
type: SiteQuality
SIO_000300: 5.083e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.62e0

VQSLOD
type: SiteQuality
SIO_000300: -1.564e0

DP
type: SiteQuality
SIO_000300: 1.668628e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.29e-1

MQ
type: SiteQuality
SIO_000300: 5.924e1

QD
type: SiteQuality
SIO_000300: 6.88e0

GenotypeQuality
all individuals: 2746
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2350
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 739
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6446
bin: 9.75e1
variant carriers: 39

GenotypeQuality
all individuals: 7040
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1775
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001200480192077e-5
allele num: 66640
num of homozygotes: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.158748551564311e-3
allele num: 8630
num of homozygotes: 0

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

African
type: Population
allele count: 20
allele frequency: 1.92789666473877e-3
allele num: 10374
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: 6
allele frequency: 3.635041802980734e-4
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.670613e6

MQRankSum
type: SiteQuality
SIO_000300: 2.77e-1

FS
type: SiteQuality
SIO_000300: 1.271e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

QD
type: SiteQuality
SIO_000300: 1.289e1

VQSLOD
type: SiteQuality
SIO_000300: 3.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.14e-1

GenotypeQuality
all individuals: 1777
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2750
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7064
bin: 6.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2358
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1006
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38390
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6417
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 741
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.032e0

VQSLOD
type: SiteQuality
SIO_000300: -1.677e0

MQ
type: SiteQuality
SIO_000300: 5.878e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.671e0

QD
type: SiteQuality
SIO_000300: 7.8e0

DP
type: SiteQuality
SIO_000300: 1.669739e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.43e-1

GenotypeQuality
all individuals: 13
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2355
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 38413
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 87
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1006
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1779
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2749
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.633911368015414e-5
allele num: 10380
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66652
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.067e0

VQSLOD
type: SiteQuality
SIO_000300: -4.32e-1

QD
type: SiteQuality
SIO_000300: 7.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.282e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.669946e6

MQRankSum
type: SiteQuality
SIO_000300: 5.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 1.730702665282105e-4
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East Asian
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South Asian
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Other
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MQRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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DP
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QD
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MQ
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InbreedingCoeff
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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East Asian
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Other
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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FS
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MQ
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InbreedingCoeff
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QD
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DP
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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DP
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VQSLOD
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FS
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Latino
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African
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Other
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South Asian
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BaseQRankSum
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DP
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QD
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MQ
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FS
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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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
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Other
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Latino
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European (Non-Finnish)
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African
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East Asian
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South Asian
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MQRankSum
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FS
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ClippingRankSum
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MQ
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QD
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Finnish)
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European (Non-Finnish)
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South Asian
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QD
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BaseQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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East Asian
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African
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European (Non-Finnish)
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MQ
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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QD
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FS
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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Other
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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ClippingRankSum
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DP
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QD
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ReadPosRankSum
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SIO_000300: -3.43e-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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African
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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InbreedingCoeff
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FS
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VQSLOD
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MQ
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QD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66694
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South Asian
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African
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Latino
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MQRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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FS
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MQ
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Latino
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Other
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66692
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.039e0

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

European (Non-Finnish)
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allele frequency: 1.499565126113427e-5
allele num: 66686
num of homozygotes: 0

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

European (Finnish)
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ReadPosRankSum
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SIO_000300: -1.002e0

BaseQRankSum
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FS
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MQRankSum
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DP
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QD
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InbreedingCoeff
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VQSLOD
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MQ
type: SiteQuality
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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
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Latino
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num of homozygotes: 0

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

European (Non-Finnish)
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African
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East Asian
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Latino
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South Asian
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Other
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DP
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FS
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InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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East Asian
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South Asian
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African
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European (Finnish)
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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QD
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FS
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ReadPosRankSum
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.999130252226854e-5
allele num: 66686
num of homozygotes: 0

QD
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MQ
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FS
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VQSLOD
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BaseQRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6610
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African
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allele frequency: 1.924187030979411e-4
allele num: 10394
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.49947518368571e-5
allele num: 66690
num of homozygotes: 0

East Asian
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allele frequency: 2.31107002542177e-4
allele num: 8654
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South Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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MQ
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FS
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DP
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VQSLOD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

East Asian
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allele count: 8
allele frequency: 9.246417013407304e-4
allele num: 8652
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

VQSLOD
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FS
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MQRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.963e1

BaseQRankSum
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InbreedingCoeff
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SIO_000300: -2.0e-4

QD
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.169e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.677263e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

BaseQRankSum
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SIO_000300: 3.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.606e1

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

European (Non-Finnish)
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allele count: 23
allele frequency: 3.449103233159379e-4
allele num: 66684
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

African
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allele count: 2
allele frequency: 1.924187030979411e-4
allele num: 10394
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.95e1

DP
type: SiteQuality
SIO_000300: 1.678375e6

MQRankSum
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SIO_000300: 1.02e-1

FS
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QD
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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SIO_000300: 3.65e0

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

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056935190793458e-5
allele num: 16510
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Latino
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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InbreedingCoeff
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VQSLOD
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FS
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MQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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DP
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BaseQRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 8654
num of homozygotes: 0

European (Finnish)
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Latino
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allele frequency: 0.0e0
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African
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South Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 6.45e-1

InbreedingCoeff
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MQRankSum
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QD
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DP
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VQSLOD
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ReadPosRankSum
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MQ
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BaseQRankSum
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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
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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Latino
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African
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European (Finnish)
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Other
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South Asian
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DP
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QD
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MQRankSum
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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Other
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 5
allele frequency: 7.498950146979423e-5
allele num: 66676
num of homozygotes: 0

European (Finnish)
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BaseQRankSum
type: SiteQuality
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QD
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FS
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SIO_000300: 1.116e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.677732e6

MQ
type: SiteQuality
SIO_000300: 5.955e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 8.58e-1

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 5.1e-2

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.677526e6

MQ
type: SiteQuality
SIO_000300: 5.955e1

GenotypeQuality
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variant carriers: 1

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.14e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.955e1

FS
type: SiteQuality
SIO_000300: 4.004e0

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
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QD
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

European (Finnish)
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allele count: 1
allele frequency: 1.519295047098146e-4
allele num: 6582
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10392
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.909e1

DP
type: SiteQuality
SIO_000300: 1.677099e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.73e0

VQSLOD
type: SiteQuality
SIO_000300: -7.427e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
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SIO_000300: 4.529e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.89e0

BaseQRankSum
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SIO_000300: 3.46e0

MQRankSum
type: SiteQuality
SIO_000300: -4.32e-1

QD
type: SiteQuality
SIO_000300: 1.049e1

GenotypeQuality
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variant carriers: 2

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.926411096127914e-4
allele num: 10382
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.92e0

FS
type: SiteQuality
SIO_000300: 4.81e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.39e-1

QD
type: SiteQuality
SIO_000300: 1.105e1

DP
type: SiteQuality
SIO_000300: 1.676691e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-2

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.63020030816641e-5
allele num: 10384
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.988e1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

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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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

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

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

East Asian
type: Population
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allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50073536032656e-5
allele num: 66634
num of homozygotes: 0

African
type: Population
allele count: 0
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num of homozygotes: 0

Other
type: Population
allele count: 0
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South Asian
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East Asian
type: Population
allele count: 0
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 4
allele frequency: 6.106870229007634e-4
allele num: 6550
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 9.22e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
SIO_000300: 1.275e1

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

Other
type: Population
allele count: 2
allele frequency: 2.207505518763797e-3
allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.658008658008658e-5
allele num: 11550
num of homozygotes: 0

African
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allele frequency: 2.889060092449923e-4
allele num: 10384
num of homozygotes: 0

East Asian
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allele count: 596
allele frequency: 6.898148148148148e-2
allele num: 8640
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European (Non-Finnish)
type: Population
allele count: 22
allele frequency: 3.301617792718432e-4
allele num: 66634
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European (Finnish)
type: Population
allele count: 21
allele frequency: 3.205128205128205e-3
allele num: 6552
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South Asian
type: Population
allele count: 35
allele frequency: 2.121469269002303e-3
allele num: 16498
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
type: SiteQuality
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DP
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VQSLOD
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 4.47e-2

ReadPosRankSum
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.263e1

GenotypeQuality
all individuals: 82
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38019
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2709
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2333
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6454
bin: 9.75e1
variant carriers: 3

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.63020030816641e-5
allele num: 10384
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.778e0

DP
type: SiteQuality
SIO_000300: 1.67897e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.927e1

FS
type: SiteQuality
SIO_000300: 6.441e0

QD
type: SiteQuality
SIO_000300: 1.211e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.46e-1

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2704
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7039
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37853
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1756
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2328
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6452
bin: 9.75e1
variant carriers: 6

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.007088364269839e-5
allele num: 66588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.533272002453235e-4
allele num: 6522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.08e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

MQ
type: SiteQuality
SIO_000300: 5.946e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.97e-1

FS
type: SiteQuality
SIO_000300: 5.47e-1

DP
type: SiteQuality
SIO_000300: 1.676568e6

MQRankSum
type: SiteQuality
SIO_000300: -7.4e-2

GenotypeQuality
all individuals: 1751
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7017
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2702
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1011
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.674531575294934e-5
allele num: 11528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502133028901039e-5
allele num: 66572
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.095e1

MQ
type: SiteQuality
SIO_000300: 5.722e1

MQRankSum
type: SiteQuality
SIO_000300: 2.88e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.351e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

DP
type: SiteQuality
SIO_000300: 1.675302e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.09e-1

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6886
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36216
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6689
bin: 9.75e1
variant carriers: 315

GenotypeQuality
all individuals: 237
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2658
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2286
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 31
allele frequency: 4.794308691617693e-3
allele num: 6466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 210
allele frequency: 3.158179685385148e-3
allele num: 66494
num of homozygotes: 0

South Asian
type: Population
allele count: 65
allele frequency: 3.957622990745251e-3
allele num: 16424
num of homozygotes: 1

African
type: Population
allele count: 5
allele frequency: 4.837461300309598e-4
allele num: 10336
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 6.681514476614699e-3
allele num: 898
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.01e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

FS
type: SiteQuality
SIO_000300: 1.98e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.9e0

QD
type: SiteQuality
SIO_000300: 1.179e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.148e0

DP
type: SiteQuality
SIO_000300: 1.672787e6

GenotypeQuality
all individuals: 6901
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2663
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6437
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 109
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1002
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36358
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504166541319455e-5
allele num: 66482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.234e1

MQRankSum
type: SiteQuality
SIO_000300: 3.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.844e0

VQSLOD
type: SiteQuality
SIO_000300: -1.316e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.67e-1

DP
type: SiteQuality
SIO_000300: 1.663397e6

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35270
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1290
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 467
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2646
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1725
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6439
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1000
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2279
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505615947484116e-5
allele num: 66418
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6430
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.106e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.043e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.22e0

DP
type: SiteQuality
SIO_000300: 1.653844e6

GenotypeQuality
all individuals: 497
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 725
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 467
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6439
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1000
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1725
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2646
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2279
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66418
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.610966057441253e-4
allele num: 11490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6430
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.22e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.043e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.653844e6

QD
type: SiteQuality
SIO_000300: 1.106e1

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

GenotypeQuality
all individuals: 211
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6439
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1000
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6828
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1725
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66418
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6430
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16198001394376e-4
allele num: 8606
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.22e0

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.73e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.106e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.043e0

DP
type: SiteQuality
SIO_000300: 1.653844e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.27e-1

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 239
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 749
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6436
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1062
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 733
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1713
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6556
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1001
bin: 9.25e1
variant carriers: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.506387081224391e-5
allele num: 66384
num of homozygotes: 0

DP
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FS
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QD
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MQ
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: 1.5e-3

BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
allele num: 16394
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 1.937984496124031e-4
allele num: 10320
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.507977199384745e-5
allele num: 66314
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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Other
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num of homozygotes: 0

Latino
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e0

FS
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MQRankSum
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

Other
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allele num: 894
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 3.017683626048645e-5
allele num: 66276
num of homozygotes: 0

African
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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QD
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FS
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MQRankSum
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DP
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InbreedingCoeff
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MQ
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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European (Non-Finnish)
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allele num: 66250
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Latino
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East Asian
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Other
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African
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MQ
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FS
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VQSLOD
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DP
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

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

European (Non-Finnish)
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South Asian
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Latino
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African
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East Asian
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Other
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BaseQRankSum
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QD
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DP
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InbreedingCoeff
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FS
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MQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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African
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MQ
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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FS
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MQRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.750390015600624e-5
allele num: 10256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65966
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16278
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.55166e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.545e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.85e-1

FS
type: SiteQuality
SIO_000300: 1.708e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.14e0

QD
type: SiteQuality
SIO_000300: 2.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.67e0

GenotypeQuality
all individuals: 1680
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.25e1
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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: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16278
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.796622097114708e-5
allele num: 11368
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65966
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.67e0

QD
type: SiteQuality
SIO_000300: 2.14e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

VQSLOD
type: SiteQuality
SIO_000300: -4.545e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.85e-1

DP
type: SiteQuality
SIO_000300: 1.55166e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.75e-1

FS
type: SiteQuality
SIO_000300: 1.708e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6334
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516116316443798e-5
allele num: 65958
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -1.073e0

MQRankSum
type: SiteQuality
SIO_000300: 8.87e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.368e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.95e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.924e0

DP
type: SiteQuality
SIO_000300: 1.548689e6

QD
type: SiteQuality
SIO_000300: 9.23e0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2831
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16210
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520542529574552e-5
allele num: 65766
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.387e0

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 3.832e0

QD
type: SiteQuality
SIO_000300: 8.470000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.42e-1

DP
type: SiteQuality
SIO_000300: 1.547565e6

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.75e1
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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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
all individuals: 42003
bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.023733510029516e-5
allele num: 66404
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.486e0

MQRankSum
type: SiteQuality
SIO_000300: -6.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.039e0

DP
type: SiteQuality
SIO_000300: 4.043803e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

VQSLOD
type: SiteQuality
SIO_000300: 5.36e-1

QD
type: SiteQuality
SIO_000300: 1.147e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 62
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2831
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66396
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21447656060238e-4
allele num: 16468
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.962e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.54e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.207e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.56e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.79e-1

DP
type: SiteQuality
SIO_000300: 4.043803e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.637e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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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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variant carriers: 2

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 2273
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.31696014828545e-4
allele num: 8632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66406
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.49e-1

QD
type: SiteQuality
SIO_000300: 1.544e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.49e-1

FS
type: SiteQuality
SIO_000300: 2.857e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

DP
type: SiteQuality
SIO_000300: 4.044149e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.07e0

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0