16-321281-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321281
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321281
    reference: chr 16
allele count: 28
allele frequency: 2.398040458368305e-4
allele num: 116762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2723C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.473C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.783C>T
  hgvsp: ENST00000397770.3:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-600G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.750C>T
  hgvsp: ENST00000359740.5:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2277G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*289C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.720C>T
  hgvsp: ENST00000316163.5:c.720C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2277G>A
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17935
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29734
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38256
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1258
  bin: 8.25e1
  variant carriers: 0
hgvs: p.His261His
num of homozygotes: 1
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-321291-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321291
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321291
    reference: chr 16
allele count: 2
allele frequency: 1.712504709387951e-5
allele num: 116788
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.740G>C
  hgvsp: ENSP00000352778.5:p.Arg247Pro
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*279G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.710G>C
  hgvsp: ENSP00000319069.5:p.Arg237Pro
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.773G>C
  hgvsp: ENSP00000380876.3:p.Arg258Pro
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2287C>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-590C>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.463G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2287C>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2713G>C
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2637
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Arg258Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

16-321291-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321291
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321291
    reference: chr 16
allele count: 1
allele frequency: 8.562523546939755e-6
allele num: 116788
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-590C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.710G>A
  hgvsp: ENSP00000319069.5:p.Arg237His
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2287C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.463G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2287C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*279G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2713G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.740G>A
  hgvsp: ENSP00000352778.5:p.Arg247His
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.773G>A
  hgvsp: ENSP00000380876.3:p.Arg258His
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28853
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7819
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36776
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg258His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

16-321292-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321292
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321292
    reference: chr 16
allele count: 2
allele frequency: 1.712475383166367e-5
allele num: 116790
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2288G>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2288G>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.462C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2712C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.739C>A
  hgvsp: ENSP00000352778.5:p.Arg247Ser
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*278C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-589G>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.772C>A
  hgvsp: ENSP00000380876.3:p.Arg258Ser
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.709C>A
  hgvsp: ENSP00000319069.5:p.Arg237Ser
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28678
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5806
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1281
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 883
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2469
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg258Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

16-321296-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321296
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321296
    reference: chr 16
allele count: 1
allele frequency: 8.556076525548445e-6
allele num: 116876
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2292G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2292G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2708C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.768C>T
  hgvsp: ENST00000397770.3:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*274C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.735C>T
  hgvsp: ENST00000359740.5:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.705C>T
  hgvsp: ENST00000316163.5:c.705C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-585G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.458C>T
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly256Gly
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD

16-321298-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321298
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321298
    reference: chr 16
allele count: 2
allele frequency: 1.712064921501823e-5
allele num: 116818
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.733G>A
  hgvsp: ENSP00000352778.5:p.Gly245Ser
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2706G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-583C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2294C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*272G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.456G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.703G>A
  hgvsp: ENSP00000319069.5:p.Gly235Ser
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.766G>A
  hgvsp: ENSP00000380876.3:p.Gly256Ser
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2294C>T
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18107
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5805
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2785
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 724
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1298
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly256Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

16-321299-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321299
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321299
    reference: chr 16
allele count: 34
allele frequency: 2.911906270875799e-4
allele num: 116762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2295G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*271C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.455C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.765C>T
  hgvsp: ENST00000397770.3:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2295G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.732C>T
  hgvsp: ENST00000359740.5:c.732C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.702C>T
  hgvsp: ENST00000316163.5:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-582G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2705C>T
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18171
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5914
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28200
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2694
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys255Cys
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

16-321303-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321303
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321303
    reference: chr 16
allele count: 1
allele frequency: 8.547154652216277e-6
allele num: 116998
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2701T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.698T>C
  hgvsp: ENSP00000319069.5:p.Phe233Ser
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.761T>C
  hgvsp: ENSP00000380876.3:p.Phe254Ser
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.728T>C
  hgvsp: ENSP00000352778.5:p.Phe243Ser
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-578A>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.451T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2299A>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2299A>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*267T>C
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Phe254Ser
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

16-321310-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321310
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321310
    reference: chr 16
allele count: 3
allele frequency: 2.563839606194236e-5
allele num: 117012
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2306G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2694C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-571G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.691C>T
  hgvsp: ENST00000316163.5:c.691C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.444C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.754C>T
  hgvsp: ENST00000397770.3:c.754C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.721C>T
  hgvsp: ENST00000359740.5:c.721C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2306G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*260C>T
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18035
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2731
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu252Leu
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

16-321328-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321328
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321328
    reference: chr 16
allele count: 3
allele frequency: 2.558809982770679e-5
allele num: 117242
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2324T>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.717-14A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.750-14A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2324T>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*256-14A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.440-14A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2676A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-553T>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.687-14A>G
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18316
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1396
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1152
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33359
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8085
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

16-321342-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321342
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321342
    reference: chr 16
allele count: 1
allele frequency: 8.503545978673106e-6
allele num: 117598
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2338G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.440-28C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-539G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2662C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.717-28C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*256-28C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.687-28C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2338G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.750-28C>T
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2074
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19031
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2357
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2921
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

16-321344-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321344
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321345
    reference: chr 16
allele count: 1
allele frequency: 8.49689863199932e-6
allele num: 117690
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.440-31dupC
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.687-31dupC
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.717-31dupC
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2659dupC
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2344dupG
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.750-31dupC
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2344dupG
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-533dupG
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*256-31dupC
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26703
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6905
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/16-321353-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321353
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321353
    reference: chr 16
allele count: 1
allele frequency: 8.47802495930548e-6
allele num: 117952
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2349A>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2349A>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.440-39T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*256-39T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2651T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.687-39T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.750-39T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.717-39T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-528A>C
  variant of: http://identifiers.org/hgnc/680
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2038
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD

16-321356-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321356
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321356
    reference: chr 16
allele count: 1
allele frequency: 8.467974121871083e-6
allele num: 118092
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-525A>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2648T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2352A>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2352A>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*255+42T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.686+42T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.439+42T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.749+42T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.716+42T>C
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26709
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

16-321358-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321358
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321358
    reference: chr 16
allele count: 1
allele frequency: 8.464676903282601e-6
allele num: 118138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2354T>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.749+40A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.716+40A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.439+40A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2646A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-523T>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.686+40A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*255+40A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2354T>C
  variant of: http://identifiers.org/hgnc/680
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8881
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

16-321369-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321369
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321369
    reference: chr 16
allele count: 1
allele frequency: 8.43355204344966e-6
allele num: 118574
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2365C>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2365C>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.686+29G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-512C>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*255+29G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.716+29G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.439+29G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.749+29G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2635G>C
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

16-321370-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321370
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321370
    reference: chr 16
allele count: 2
allele frequency: 1.686198465559396e-5
allele num: 118610
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*255+28A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2366T>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.749+28A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.686+28A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.439+28A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2634A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.716+28A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2366T>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-511T>C
  variant of: http://identifiers.org/hgnc/680
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1090
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9158
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3513
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3316
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-321377-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321377
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321377
    reference: chr 16
allele count: 1
allele frequency: 8.414391976035812e-6
allele num: 118844
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-504G>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.686+21C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2627C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.439+21C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2373G>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2373G>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.716+21C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*255+21C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.749+21C>G
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3381
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-321380-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321380
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321380
    reference: chr 16
allele count: 2
allele frequency: 1.681378730559058e-5
allele num: 118950
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.749+18T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.439+18T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2376A>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*255+18T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2624T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.716+18T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.686+18T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2376A>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-501A>G
  variant of: http://identifiers.org/hgnc/680
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7921
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1264
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1854
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD

16-321383-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321383
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321383
    reference: chr 16
allele count: 1
allele frequency: 8.396869646995599e-6
allele num: 119092
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.686+15G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2379C>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2621G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-498C>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.749+15G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.716+15G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2379C>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.439+15G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*255+15G>C
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20744
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3444
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37783
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS

16-321384-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321384
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321384
    reference: chr 16
allele count: 1
allele frequency: 8.395318770253707e-6
allele num: 119114
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.749+14G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.716+14G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.686+14G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.439+14G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2620G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-497C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*255+14G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2380C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2380C>T
  variant of: http://identifiers.org/hgnc/680
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8044
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9401
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37489
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1875
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

16-321386-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321386
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321386
    reference: chr 16
allele count: 5
allele frequency: 4.195546008357528e-5
allele num: 119174
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.686+12G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.716+12G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2618G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.749+12G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.439+12G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2382C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2382C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*255+12G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-495C>T
  variant of: http://identifiers.org/hgnc/680
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20802
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1888
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37744
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/16-321387-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321387
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321386
    reference: chr 16
allele count: 1
allele frequency: 8.388558006878617e-6
allele num: 119210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.686+10delG
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2387delC
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*255+10delG
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.439+10delG
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.749+10delG
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2387delC
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2616delG
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.716+10delG
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-490delC
  variant of: http://identifiers.org/hgnc/680
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8091
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3464
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1085
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: AC
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/16-321390-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321390
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321390
    reference: chr 16
allele count: 2
allele frequency: 1.676333523317799e-5
allele num: 119308
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*255+8G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2614G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.716+8G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-491C>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.686+8G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.749+8G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2386C>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2386C>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.439+8G>T
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1897
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3707
  bin: 7.25e1
  variant carriers: 0
hgvs: c.749+8G>T
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-321395-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321395
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321395
    reference: chr 16
allele count: 1
allele frequency: 8.368901163277262e-6
allele num: 119490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2609G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.749+3G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*255+3G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.686+3G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.439+3G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.716+3G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2391C>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-486C>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2391C>A
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
hgvs: c.749+3G>T
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

16-321397-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321397
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321397
    reference: chr 16
allele count: 7
allele frequency: 5.855584554640969e-5
allele num: 119544
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.716+1G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.439+1G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.749+1G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2393C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-484C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.686+1G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2393C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2607G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*255+1G>A
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 2.25e1
  variant carriers: 0
hgvs: c.749+1G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

16-321398-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321398
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321398
    reference: chr 16
allele count: 1
allele frequency: 8.362462577979963e-6
allele num: 119582
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.749C>A
  hgvsp: ENSP00000380876.3:p.Ala250Glu
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*255C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2394G>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2606C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-483G>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.686C>A
  hgvsp: ENSP00000319069.5:p.Ala229Glu
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.716C>A
  hgvsp: ENSP00000352778.5:p.Ala239Glu
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.439C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2394G>T
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8251
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3511
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala250Glu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

16-321400-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321400
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321400
    reference: chr 16
allele count: 1
allele frequency: 8.356592515835743e-6
allele num: 119666
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2396C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2604G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.714G>A
  hgvsp: ENST00000359740.5:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.684G>A
  hgvsp: ENST00000316163.5:c.684G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.437G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-481C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.747G>A
  hgvsp: ENST00000397770.3:c.747G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2396C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*253G>A
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21120
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8263
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9588
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
hgvs: c.747G>A
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/16-321404-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321404
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321404
    reference: chr 16
allele count: 5
allele frequency: 4.174598403633571e-5
allele num: 119772
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2400A>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2600T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-477A>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*249T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.433T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.743T>G
  hgvsp: ENSP00000380876.3:p.Leu248Arg
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.680T>G
  hgvsp: ENSP00000319069.5:p.Leu227Arg
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.710T>G
  hgvsp: ENSP00000352778.5:p.Leu237Arg
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2400A>C
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21189
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27436
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8281
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu248Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/16-321411-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321411
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321411
    reference: chr 16
allele count: 1
allele frequency: 8.340283569641367e-6
allele num: 119900
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2407C>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2593G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-470C>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2407C>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.673G>T
  hgvsp: ENSP00000319069.5:p.Val225Phe
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.703G>T
  hgvsp: ENSP00000352778.5:p.Val235Phe
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.736G>T
  hgvsp: ENSP00000380876.3:p.Val246Phe
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.426G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*242G>T
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9647
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val246Phe
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP

16-321411-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321411
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321411
    reference: chr 16
allele count: 3
allele frequency: 2.50208507089241e-5
allele num: 119900
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.736G>A
  hgvsp: ENSP00000380876.3:p.Val246Ile
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.426G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-470C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2407C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2593G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.703G>A
  hgvsp: ENSP00000352778.5:p.Val235Ile
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.673G>A
  hgvsp: ENSP00000319069.5:p.Val225Ile
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*242G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2407C>T
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9647
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val246Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

16-321412-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321412
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321412
    reference: chr 16
allele count: 1
allele frequency: 8.337502084375522e-6
allele num: 119940
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.425C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.735C>T
  hgvsp: ENST00000397770.3:c.735C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2592C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*241C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.672C>T
  hgvsp: ENST00000316163.5:c.672C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.702C>T
  hgvsp: ENST00000359740.5:c.702C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2408G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-469G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2408G>A
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38588
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3536
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser245Ser
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum

16-321415-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321415
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321415
    reference: chr 16
allele count: 1
allele frequency: 8.332500083325001e-6
allele num: 120012
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*238C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.422C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.732C>T
  hgvsp: ENST00000397770.3:c.732C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.669C>T
  hgvsp: ENST00000316163.5:c.669C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.699C>T
  hgvsp: ENST00000359740.5:c.699C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2589C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-466G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2411G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2411G>A
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27480
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8326
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38624
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser244Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff

16-321424-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321424
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321424
    reference: chr 16
allele count: 67
allele frequency: 5.578405741594924e-4
allele num: 120106
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*229A>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.690A>T
  hgvsp: ENST00000359740.5:c.690A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2580A>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-457T>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2420T>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2420T>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.660A>T
  hgvsp: ENST00000316163.5:c.660A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.723A>T
  hgvsp: ENST00000397770.3:c.723A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.413A>T
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27419
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8351
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21386
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3550
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg241Arg
num of homozygotes: 1
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ

16-321425-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321425
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321425
    reference: chr 16
allele count: 1
allele frequency: 8.324869715788949e-6
allele num: 120122
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*228G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2421C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.412G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-456C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2421C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2579G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.722G>A
  hgvsp: ENSP00000380876.3:p.Arg241Gln
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.689G>A
  hgvsp: ENSP00000352778.5:p.Arg230Gln
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.659G>A
  hgvsp: ENSP00000319069.5:p.Arg220Gln
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3802
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg241Gln
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

16-321425-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321425
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321424
    reference: chr 16
allele count: 1
allele frequency: 8.324869715788949e-6
allele num: 120122
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-453delG
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.721delC
  hgvsp: ENSP00000380876.3:p.Arg241GlufsTer2
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.411delC
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.658delC
  hgvsp: ENSP00000319069.5:p.Arg220GlufsTer2
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2578delC
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.688delC
  hgvsp: ENSP00000352778.5:p.Arg230GlufsTer2
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*227delC
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2424delG
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2424delG
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21404
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg241GlufsTer2
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: CG
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-321426-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321426
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321426
    reference: chr 16
allele count: 7
allele frequency: 5.826147751106968e-5
allele num: 120148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2422G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2578C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.688C>T
  hgvsp: ENSP00000352778.5:p.Arg230Ter
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.411C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.721C>T
  hgvsp: ENSP00000380876.3:p.Arg241Ter
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*227C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.658C>T
  hgvsp: ENSP00000319069.5:p.Arg220Ter
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-455G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2422G>A
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21399
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1965
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38598
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg241Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

16-321426-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321426
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321426
    reference: chr 16
allele count: 1
allele frequency: 8.323068215867098e-6
allele num: 120148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-455G>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.411C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.688C>G
  hgvsp: ENSP00000352778.5:p.Arg230Gly
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2422G>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*227C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2578C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2422G>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.721C>G
  hgvsp: ENSP00000380876.3:p.Arg241Gly
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.658C>G
  hgvsp: ENSP00000319069.5:p.Arg220Gly
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3795
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg241Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

16-321427-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321427
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321427
    reference: chr 16
allele count: 1
allele frequency: 8.321544478655239e-6
allele num: 120170
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2423G>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-454G>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.687C>G
  hgvsp: ENST00000359740.5:c.687C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*226C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2577C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.410C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.720C>G
  hgvsp: ENST00000397770.3:c.720C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.657C>G
  hgvsp: ENST00000316163.5:c.657C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2423G>C
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr240Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

16-321427-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321427
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321427
    reference: chr 16
allele count: 2
allele frequency: 1.664308895731048e-5
allele num: 120170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2423G>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.410C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2423G>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.687C>A
  hgvsp: ENST00000359740.5:c.687C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.657C>A
  hgvsp: ENST00000316163.5:c.657C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*226C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-454G>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.720C>A
  hgvsp: ENST00000397770.3:c.720C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2577C>A
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8396
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9734
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 38617
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr240Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

16-321428-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321428
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321428
    reference: chr 16
allele count: 3
allele frequency: 2.49613099695472e-5
allele num: 120186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.656C>A
  hgvsp: ENSP00000319069.5:p.Thr219Asn
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.719C>A
  hgvsp: ENSP00000380876.3:p.Thr240Asn
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.409C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*225C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.686C>A
  hgvsp: ENSP00000352778.5:p.Thr229Asn
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2576C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-453G>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2424G>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2424G>T
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8395
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1971
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr240Asn
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD

16-321436-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321436
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321436
    reference: chr 16
allele count: 1
allele frequency: 8.315593400745077e-6
allele num: 120256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.401G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.711G>A
  hgvsp: ENST00000397770.3:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.678G>A
  hgvsp: ENST00000359740.5:c.678G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2432C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2432C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*217G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.648G>A
  hgvsp: ENST00000316163.5:c.648G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-445C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2568G>A
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8430
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3570
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3822
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 749
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu237Leu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

16-321440-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321440
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321440
    reference: chr 16
allele count: 52
allele frequency: 4.322886357968243e-4
allele num: 120290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.674C>T
  hgvsp: ENSP00000352778.5:p.Ala225Val
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2436G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*213C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.644C>T
  hgvsp: ENSP00000319069.5:p.Ala215Val
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.397C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2436G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-441G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2564C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.707C>T
  hgvsp: ENSP00000380876.3:p.Ala236Val
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21497
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27250
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8449
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala236Val
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

16-321455-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321455
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321455
    reference: chr 16
allele count: 1
allele frequency: 8.30675172780436e-6
allele num: 120384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-426T>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2451T>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2451T>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2549A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.659A>G
  hgvsp: ENSP00000352778.5:p.Glu220Gly
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.629A>G
  hgvsp: ENSP00000319069.5:p.Glu210Gly
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.692A>G
  hgvsp: ENSP00000380876.3:p.Glu231Gly
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.382A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*198A>G
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21575
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 378
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1974
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu231Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum

16-321456-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321456
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321456
    reference: chr 16
allele count: 2
allele frequency: 1.661295145695584e-5
allele num: 120388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.381G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*197G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-425C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.658G>A
  hgvsp: ENSP00000352778.5:p.Glu220Lys
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.691G>A
  hgvsp: ENSP00000380876.3:p.Glu231Lys
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2452C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.628G>A
  hgvsp: ENSP00000319069.5:p.Glu210Lys
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2548G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2452C>T
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27204
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu231Lys
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

16-321457-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321457
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321457
    reference: chr 16
allele count: 1
allele frequency: 8.30592378484335e-6
allele num: 120396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2453G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*196C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2547C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2453G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.690C>T
  hgvsp: ENST00000397770.3:c.690C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-424G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.627C>T
  hgvsp: ENST00000316163.5:c.627C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.380C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.657C>T
  hgvsp: ENST00000359740.5:c.657C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3574
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38618
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.25e1
  variant carriers: 0
hgvs: c.690C>T
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD

16-321457-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321457
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321457
    reference: chr 16
allele count: 1
allele frequency: 8.30592378484335e-6
allele num: 120396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*196C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2547C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2453G>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-424G>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.627C>G
  hgvsp: ENSP00000319069.5:p.Ile209Met
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.690C>G
  hgvsp: ENSP00000380876.3:p.Ile230Met
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.380C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.657C>G
  hgvsp: ENSP00000352778.5:p.Ile219Met
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2453G>C
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1732
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3574
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile230Met
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: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-321462-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321462
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321462
    reference: chr 16
allele count: 2
allele frequency: 1.660715768496222e-5
allele num: 120430
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.378-3T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.688-3T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*194-3T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2458A>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2542T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.655-3T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.625-3T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2458A>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-419A>C
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27179
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3837
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9745
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
hgvs: c.688-3T>G
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

16-321462-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321462
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321462
    reference: chr 16
allele count: 11
allele frequency: 9.133936726729221e-5
allele num: 120430
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*194-3T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2458A>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2458A>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.378-3T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-419A>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.655-3T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.688-3T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2542T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.625-3T>C
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1730
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27179
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21593
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9745
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
hgvs: c.688-3T>C
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

16-321465-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321465
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321465
    reference: chr 16
allele count: 258
allele frequency: 2.142181039206895e-3
allele num: 120438
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.378-6T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-416A>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2539T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.688-6T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.625-6T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2461A>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2461A>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*194-6T>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.655-6T>C
  variant of: http://identifiers.org/hgnc/9993
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8463
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 21524
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 27049
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 4.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38485
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
hgvs: c.688-6T>C
num of homozygotes: 6
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

16-321466-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321466
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321466
    reference: chr 16
allele count: 1
allele frequency: 8.302751531857658e-6
allele num: 120442
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*194-7A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2462T>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.378-7A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.625-7A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-415T>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.655-7A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2538A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.688-7A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2462T>C
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9734
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 2.25e1
  variant carriers: 0
hgvs: c.688-7A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

16-321467-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321467
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321467
    reference: chr 16
allele count: 1
allele frequency: 8.301924386072691e-6
allele num: 120454
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.378-8C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2463G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-414G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*194-8C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.655-8C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.688-8C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2537C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.625-8C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2463G>A
  variant of: http://identifiers.org/hgnc/680
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1761
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8514
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
hgvs: c.688-8C>T
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

16-321470-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321470
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321470
    reference: chr 16
allele count: 3
allele frequency: 2.490577315821807e-5
allele num: 120454
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-411G>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.625-11C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2534C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2466G>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.655-11C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.688-11C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*194-11C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.378-11C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2466G>C
  variant of: http://identifiers.org/hgnc/680
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9738
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

16-321470-GGGCCTGTGAGTC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321470
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321458
    reference: chr 16
allele count: 2
allele frequency: 1.660384877214538e-5
allele num: 120454
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  variant of: http://identifiers.org/hgnc/680
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3579
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9738
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: GGGCCTGTGAGTC
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

16-321471-GGCCTGTGAGT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321471
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321461
    reference: chr 16
allele count: 1
allele frequency: 8.301786544464368e-6
allele num: 120456
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21544
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1985
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 889
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
reference allele: GGCCTGTGAGT
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

16-321474-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321474
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321474
    reference: chr 16
allele count: 1028
allele frequency: 8.533103127697722e-3
allele num: 120472
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2470C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2530G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*194-15G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.655-15G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-407C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.378-15G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.625-15G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2470C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.688-15G>A
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21188
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26606
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.75e1
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 8394
  bin: 3.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.75e1
  variant carriers: 194
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 5.75e1
  variant carriers: 107
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.75e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 3.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 74
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 8.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.25e1
  variant carriers: 86
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3772
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 21
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-321479-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321479
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321479
    reference: chr 16
allele count: 4
allele frequency: 3.319557171073379e-5
allele num: 120498
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.688-20T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.378-20T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2475A>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2525T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2475A>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-402A>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*194-20T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.625-20T>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.655-20T>G
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 730
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9638
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

16-321480-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321480
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321480
    reference: chr 16
allele count: 4
allele frequency: 3.319777574902481e-5
allele num: 120490
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.625-21C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*194-21C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2476G>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.688-21C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.655-21C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.378-21C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2524C>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-401G>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2476G>T
  variant of: http://identifiers.org/hgnc/680
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8479
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3541
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

16-321486-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321486
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321486
    reference: chr 16
allele count: 2
allele frequency: 1.659668398254029e-5
allele num: 120506
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*194-27A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2482T>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2518A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.378-27A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-395T>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.688-27A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.625-27A>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2482T>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.655-27A>G
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26557
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD

16-321488-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321488
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321488
    reference: chr 16
allele count: 3
allele frequency: 2.489172101359088e-5
allele num: 120522
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.625-29G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2484C>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.688-29G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.655-29G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-393C>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2484C>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*194-29G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.378-29G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2516G>C
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8482
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21278
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 736
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 621
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP

16-321489-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321489
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321489
    reference: chr 16
allele count: 29
allele frequency: 2.406239628277464e-4
allele num: 120520
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.378-30G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2485C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.625-30G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2515G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.655-30G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2485C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-392C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*194-30G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.688-30G>A
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 21260
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37925
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

16-321490-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321490
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321490
    reference: chr 16
allele count: 17
allele frequency: 1.410577673044691e-4
allele num: 120518
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.655-31C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2514C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*194-31C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.688-31C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2486G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.378-31C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2486G>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.625-31C>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-391G>A
  variant of: http://identifiers.org/hgnc/680
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21273
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3540
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37957
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9647
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ

16-321498-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321498
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321498
    reference: chr 16
allele count: 1
allele frequency: 8.292974192264313e-6
allele num: 120584
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.655-39C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.378-39C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2494G>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.625-39C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2506C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*194-39C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.688-39C>G
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2494G>C
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-383G>C
  variant of: http://identifiers.org/hgnc/680
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26541
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8510
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS

16-321503-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321503
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321503
    reference: chr 16
allele count: 1
allele frequency: 8.292011476143882e-6
allele num: 120598
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2499C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-378C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2501G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.654+36G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.377+36G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2499C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.687+36G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.624+36G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*193+36G>A
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

16-321506-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321506
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321506
    reference: chr 16
allele count: 6
allele frequency: 4.974629390110437e-5
allele num: 120612
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2498G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-375C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2502C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2502C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.624+33G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.377+33G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.687+33G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.654+33G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*193+33G>A
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38061
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-321510-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321510
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321510
    reference: chr 16
allele count: 47
allele frequency: 3.896211555997679e-4
allele num: 120630
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.654+29G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2506C>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-371C>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.377+29G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.624+29G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2494G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2506C>A
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.687+29G>T
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*193+29G>T
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 21322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26513
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3545
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

16-321512-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321512
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321512
    reference: chr 16
allele count: 1
allele frequency: 8.288712431410904e-6
allele num: 120646
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.624+27G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*193+27G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2492G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2508C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.377+27G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-369C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2508C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.687+27G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.654+27G>A
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8516
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38050
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3790
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9675
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum

16-321513-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321513
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321513
    reference: chr 16
allele count: 1
allele frequency: 8.288437629506838e-6
allele num: 120650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2491G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.624+26G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.377+26G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-368C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.654+26G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2509C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2509C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*193+26G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.687+26G>A
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8522
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21340
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-321516-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321516
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321516
    reference: chr 16
allele count: 2
allele frequency: 1.657330372236402e-5
allele num: 120676
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2512C>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*193+23G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.654+23G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.624+23G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-365C>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2488G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.687+23G>C
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2512C>G
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.377+23G>C
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2010
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

16-321517-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 321517
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 321517
    reference: chr 16
allele count: 1
allele frequency: 8.287475966319697e-6
allele num: 120664
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000397395
  ensembl transcript: ENST00000435035
  gene symbol: ARHGDIG
  hgvsc: ENST00000435035.1:c.169+2513C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl transcript: ENST00000464609
  gene symbol: ARHGDIG
  hgvsc: ENST00000464609.1:n.25-364C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000477143
  gene symbol: RGS11
  hgvsc: ENST00000477143.1:n.2487G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000168869
  ensembl transcript: ENST00000168869
  gene symbol: RGS11
  hgvsc: ENST00000168869.8:c.*193+22G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl transcript: ENST00000481672
  gene symbol: RGS11
  hgvsc: ENST00000481672.1:n.377+22G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000380876
  ensembl transcript: ENST00000397770
  gene symbol: RGS11
  hgvsc: ENST00000397770.3:c.687+22G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000242173
  ensembl protein: ENSP00000408037
  ensembl transcript: ENST00000412541
  gene symbol: ARHGDIG
  hgvsc: ENST00000412541.1:c.169+2513C>T
  variant of: http://identifiers.org/hgnc/680
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000352778
  ensembl transcript: ENST00000359740
  gene symbol: RGS11
  hgvsc: ENST00000359740.5:c.654+22G>A
  variant of: http://identifiers.org/hgnc/9993
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000076344
  ensembl protein: ENSP00000319069
  ensembl transcript: ENST00000316163
  gene symbol: RGS11
  hgvsc: ENST00000316163.5:c.624+22G>A
  variant of: http://identifiers.org/hgnc/9993
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 790
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 7880
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2579
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 9.75e1
variant carriers: 26

GenotypeQuality
all individuals: 2760
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 723
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.763979537837361e-4
allele num: 11338
num of homozygotes: 0

African
type: Population
allele count: 24
allele frequency: 2.491177081170853e-3
allele num: 9634
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.116235587410408e-5
allele num: 64180
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5828
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.44792e6

FS
type: SiteQuality
SIO_000300: 1.759e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.17e-1

QD
type: SiteQuality
SIO_000300: 1.259e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.79e-1

GenotypeQuality
all individuals: 490
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2474
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7819
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64152
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5832
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.068252326783868e-4
allele num: 9670
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16392
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11332
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.374e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

DP
type: SiteQuality
SIO_000300: 1.445487e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.0e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

QD
type: SiteQuality
SIO_000300: 1.179e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.94e-1

GenotypeQuality
all individuals: 138
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 916
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variant carriers: 0

GenotypeQuality
all individuals: 1280
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9670
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64152
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11332
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5832
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16767865483419e-4
allele num: 8564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.445487e6

FS
type: SiteQuality
SIO_000300: 3.374e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.78e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-1

QD
type: SiteQuality
SIO_000300: 1.179e1

GenotypeQuality
all individuals: 36247
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 934
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 487
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GenotypeQuality
all individuals: 98
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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: 2

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 436
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variant carriers: 0

GenotypeQuality
all individuals: 2642
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11330
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.066969822240595e-4
allele num: 9676
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64138
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.258e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.62e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.5e-1

DP
type: SiteQuality
SIO_000300: 1.445644e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-2

GenotypeQuality
all individuals: 2672
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2782
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 943
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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
all individuals: 549
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 457
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variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 2507
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variant carriers: 0

GenotypeQuality
all individuals: 1290
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5864
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11336
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -4.004e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.925e1

DP
type: SiteQuality
SIO_000300: 1.445701e6

ClippingRankSum
type: SiteQuality
SIO_000300: 5.31e-1

QD
type: SiteQuality
SIO_000300: 1.528e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.4e-1

GenotypeQuality
all individuals: 441
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2517
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 982
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2671
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
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variant carriers: 2

GenotypeQuality
all individuals: 503
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variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7843
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.117401334247771e-5
allele num: 64156
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16388
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5846
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11332
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.65e0

FS
type: SiteQuality
SIO_000300: 4.24e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.445866e6

QD
type: SiteQuality
SIO_000300: 1.02e1

GenotypeQuality
all individuals: 978
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 820
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 493
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variant carriers: 0

GenotypeQuality
all individuals: 1294
bin: 8.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 33

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 36360
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2486
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9682
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5854
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.764602082230457e-4
allele num: 11334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 32
allele frequency: 4.991109586049849e-4
allele num: 64114
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.87e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

QD
type: SiteQuality
SIO_000300: 1.343e1

DP
type: SiteQuality
SIO_000300: 1.449205e6

GenotypeQuality
all individuals: 836
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 84
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7925
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GenotypeQuality
all individuals: 2840
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5882
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.55671098103926e-5
allele num: 64238
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11340
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9718
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

QD
type: SiteQuality
SIO_000300: 1.066e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

FS
type: SiteQuality
SIO_000300: 2.167e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.05e-1

DP
type: SiteQuality
SIO_000300: 1.445859e6

MQRankSum
type: SiteQuality
SIO_000300: -1.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

GenotypeQuality
all individuals: 1334
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
all individuals: 377
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GenotypeQuality
all individuals: 473
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variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 35520
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variant carriers: 0

GenotypeQuality
all individuals: 508
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GenotypeQuality
all individuals: 2839
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variant carriers: 0

GenotypeQuality
all individuals: 2560
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.827262760384943e-4
allele num: 16418
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.444939e6

QD
type: SiteQuality
SIO_000300: 1.207e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.14e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.42e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

GenotypeQuality
all individuals: 55
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 572
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1122
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9758
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8564
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.664324139432196e-5
allele num: 64318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5986
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.4e-2

DP
type: SiteQuality
SIO_000300: 1.452087e6

MQRankSum
type: SiteQuality
SIO_000300: -2.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.87e-1

FS
type: SiteQuality
SIO_000300: 7.018e0

VQSLOD
type: SiteQuality
SIO_000300: 6.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

QD
type: SiteQuality
SIO_000300: 1.394e1

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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bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16438
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.01419878296146e-4
allele num: 9860
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6040
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64456
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.68e0

DP
type: SiteQuality
SIO_000300: 1.474883e6

MQ
type: SiteQuality
SIO_000300: 5.859e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e0

FS
type: SiteQuality
SIO_000300: 1.591e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.075e0

VQSLOD
type: SiteQuality
SIO_000300: -3.29e0

MQRankSum
type: SiteQuality
SIO_000300: -1.68e0

QD
type: SiteQuality
SIO_000300: 1.874e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 414
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6040
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64514
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.011531458628363e-4
allele num: 9886
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11386
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.27e-1

FS
type: SiteQuality
SIO_000300: 1.406e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

MQ
type: SiteQuality
SIO_000300: 6.033e1

DP
type: SiteQuality
SIO_000300: 1.477938e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: 1.59e0

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e0

QD
type: SiteQuality
SIO_000300: 1.011e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3095
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6094
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.163873370577281e-4
allele num: 8592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9924
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64634
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.938e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.93e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.243e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.48e-1

DP
type: SiteQuality
SIO_000300: 1.494108e6

MQRankSum
type: SiteQuality
SIO_000300: 3.29e-1

FS
type: SiteQuality
SIO_000300: 1.4e0

QD
type: SiteQuality
SIO_000300: 1.81e1

GenotypeQuality
all individuals: 285
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1948
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 400
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.005429318318922e-4
allele num: 9946
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6096
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64716
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.896e1

MQRankSum
type: SiteQuality
SIO_000300: -7.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

DP
type: SiteQuality
SIO_000300: 1.499608e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: -6.326000000000001e-1

QD
type: SiteQuality
SIO_000300: 8.029999999999999e0

GenotypeQuality
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bin: 9.75e1
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
all individuals: 1899
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.005227181342983e-4
allele num: 9948
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64732
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6116
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.07e-1

FS
type: SiteQuality
SIO_000300: 2.6535e1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.501854e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

QD
type: SiteQuality
SIO_000300: 1.385e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10034
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11454
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64962
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6176
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.971e1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.15e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.087e0

BaseQRankSum
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SIO_000300: 1.82e-1

QD
type: SiteQuality
SIO_000300: 1.203e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

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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bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10046
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.077585941587419e-5
allele num: 64986
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 9.46e-1

FS
type: SiteQuality
SIO_000300: 1.749e0

MQRankSum
type: SiteQuality
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BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 1.518597e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e-1

ReadPosRankSum
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 139
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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
variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.535249324490297e-5
allele num: 65136
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

European (Finnish)
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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

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

FS
type: SiteQuality
SIO_000300: 9.21e-1

DP
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VQSLOD
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ClippingRankSum
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QD
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MQ
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

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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variant carriers: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.067861087249969e-5
allele num: 65192
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10080
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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MQ
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BaseQRankSum
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6266
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.532050496384361e-5
allele num: 65272
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.96e-1

QD
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MQ
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DP
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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SIO_000300: 4.92e-1

BaseQRankSum
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SIO_000300: -6.0e-1

FS
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SIO_000300: 6.62e-1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6276
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65280
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10100
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.70170553428472e-5
allele num: 11492
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.85e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.292e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -4.511e-1

DP
type: SiteQuality
SIO_000300: 1.537796e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.92e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.655560999510044e-5
allele num: 65312
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
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SIO_000300: -4.0e-4

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.665e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e-1

VQSLOD
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.939e1

DP
type: SiteQuality
SIO_000300: 1.53949e6

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

East Asian
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allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

South 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
allele num: 65338
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
type: Population
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQ
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ReadPosRankSum
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DP
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FS
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ClippingRankSum
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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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Other
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African
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East Asian
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South Asian
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Latino
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European (Non-Finnish)
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allele num: 65388
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European (Finnish)
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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QD
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BaseQRankSum
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DP
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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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South Asian
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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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East Asian
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European (Non-Finnish)
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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DP
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MQRankSum
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FS
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MQ
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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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European (Non-Finnish)
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allele num: 65512
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Other
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East Asian
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South Asian
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African
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allele num: 10152
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European (Finnish)
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Latino
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BaseQRankSum
type: SiteQuality
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QD
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InbreedingCoeff
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 1.743e0

DP
type: SiteQuality
SIO_000300: 1.549182e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65544
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -8.74e-1

QD
type: SiteQuality
SIO_000300: 1.267e1

FS
type: SiteQuality
SIO_000300: 1.785e0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 6.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.47e-1

DP
type: SiteQuality
SIO_000300: 1.550086e6

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 153
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 50
bin: 4.25e1
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GenotypeQuality
all individuals: 560
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10168
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 9.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.153e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.926e0

VQSLOD
type: SiteQuality
SIO_000300: -6.281e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

FS
type: SiteQuality
SIO_000300: 3.93e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

DP
type: SiteQuality
SIO_000300: 1.551527e6

GenotypeQuality
all individuals: 3521
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 3755
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65644
num of homozygotes: 0

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

African
type: Population
allele count: 5
allele frequency: 4.912556494399686e-4
allele num: 10178
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.68e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.49e-1

DP
type: SiteQuality
SIO_000300: 1.553647e6

MQ
type: SiteQuality
SIO_000300: 5.961e1

VQSLOD
type: SiteQuality
SIO_000300: 5.580000000000001e-1

QD
type: SiteQuality
SIO_000300: 9.85e0

GenotypeQuality
all individuals: 83
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variant carriers: 0

GenotypeQuality
all individuals: 565
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variant carriers: 0

GenotypeQuality
all individuals: 14
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 710
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variant carriers: 1

GenotypeQuality
all individuals: 3536
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65714
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.809691975671964e-5
allele num: 10194
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.3e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

FS
type: SiteQuality
SIO_000300: 5.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
SIO_000300: 1.002e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.05e-1

DP
type: SiteQuality
SIO_000300: 1.556518e6

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 14
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GenotypeQuality
all individuals: 83
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GenotypeQuality
all individuals: 75
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3767
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.565237240161914e-5
allele num: 65714
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.556518e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -4.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.78e-1

QD
type: SiteQuality
SIO_000300: 1.002e1

FS
type: SiteQuality
SIO_000300: 5.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.05e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 11
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 41
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GenotypeQuality
all individuals: 567
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65732
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 9.710000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: -4.669e-1

DP
type: SiteQuality
SIO_000300: 1.557448e6

FS
type: SiteQuality
SIO_000300: 1.503e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.851e1

MQRankSum
type: SiteQuality
SIO_000300: 5.31e-1

GenotypeQuality
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bin: 9.75e1
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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bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.520496289989052e-5
allele num: 65768
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.218e0

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

QD
type: SiteQuality
SIO_000300: 9.779999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: -6.482e-1

DP
type: SiteQuality
SIO_000300: 1.558456e6

MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.63e-1

FS
type: SiteQuality
SIO_000300: 4.623e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 780
bin: 9.75e1
variant carriers: 66

GenotypeQuality
all individuals: 3799
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 52
allele frequency: 7.902255182055802e-4
allele num: 65804
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 15
allele frequency: 2.295684113865932e-3
allele num: 6534
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.01e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.34e0

DP
type: SiteQuality
SIO_000300: 1.562333e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.277e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.29e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 738
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GenotypeQuality
all individuals: 26
bin: 1.25e1
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GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
all individuals: 74
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variant carriers: 0

GenotypeQuality
all individuals: 691
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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: 7.75e1
variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6534
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65810
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

East Asian
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allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

InbreedingCoeff
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FS
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MQ
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ClippingRankSum
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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DP
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ReadPosRankSum
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SIO_000300: 2.81e-1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65810
num of homozygotes: 0

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

European (Finnish)
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allele count: 1
allele frequency: 1.530456075910621e-4
allele num: 6534
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10232
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
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FS
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DP
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QD
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.81e-1

ClippingRankSum
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SIO_000300: 5.04e-1

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

Latino
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allele frequency: 8.673026886383348e-5
allele num: 11530
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.519387383007172e-5
allele num: 65816
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

African
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allele count: 4
allele frequency: 3.907013088493846e-4
allele num: 10238
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.13e-1

FS
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SIO_000300: 1.772e0

MQ
type: SiteQuality
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QD
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VQSLOD
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MQRankSum
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ClippingRankSum
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DP
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SIO_000300: 1.563263e6

ReadPosRankSum
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SIO_000300: 5.92e-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: 10238
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65816
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.563263e6

MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-1

BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

FS
type: SiteQuality
SIO_000300: 1.772e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

QD
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MQ
type: SiteQuality
SIO_000300: 5.952e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.673026886383348e-5
allele num: 11530
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10244
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65824
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6546
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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QD
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BaseQRankSum
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DP
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FS
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ReadPosRankSum
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SIO_000300: 1.28e0

MQRankSum
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ClippingRankSum
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SIO_000300: -1.414e0

VQSLOD
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SIO_000300: 4.55e-1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

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

African
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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: 1.212121212121212e-4
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65824
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

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

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

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 892
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 frequency: 0.0e0
allele num: 16500
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.556915879332868e-5
allele num: 65834
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.144e0

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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MQ
type: SiteQuality
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DP
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MQRankSum
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 8.110000000000001e-1

ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
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allele num: 892
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
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South Asian
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allele frequency: 6.059871530723549e-5
allele num: 16502
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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Latino
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ReadPosRankSum
type: SiteQuality
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MQ
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MQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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FS
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BaseQRankSum
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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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variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.948937828883259e-4
allele num: 10262
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 46
allele frequency: 6.980696855651329e-4
allele num: 65896
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

South Asian
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allele count: 2
allele frequency: 1.21197430614471e-4
allele num: 16502
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.94e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

FS
type: SiteQuality
SIO_000300: 1.757e0

DP
type: SiteQuality
SIO_000300: 1.567749e6

MQRankSum
type: SiteQuality
SIO_000300: 2.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.227e1

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

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: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516392199678525e-5
allele num: 65946
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.749e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: -4.61e-2

FS
type: SiteQuality
SIO_000300: 2.772e0

MQRankSum
type: SiteQuality
SIO_000300: -3.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.567614e6

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.997e0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.733307377846993e-5
allele num: 10274
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.668515950069348e-5
allele num: 11536
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65952
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

QD
type: SiteQuality
SIO_000300: 1.192e1

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.23e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.55e-1

DP
type: SiteQuality
SIO_000300: 1.567947e6

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 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: 892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65954
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.749e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.57e-1

DP
type: SiteQuality
SIO_000300: 1.568223e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.67e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
type: SiteQuality
SIO_000300: 1.36e-1

QD
type: SiteQuality
SIO_000300: 1.417e1

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

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

GenotypeQuality
all individuals: 1974
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516208266367468e-5
allele num: 65954
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e-1

DP
type: SiteQuality
SIO_000300: 1.568223e6

MQRankSum
type: SiteQuality
SIO_000300: 1.36e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.66e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

QD
type: SiteQuality
SIO_000300: 1.417e1

FS
type: SiteQuality
SIO_000300: 1.749e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.57e-1

GenotypeQuality
all individuals: 111
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variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65972
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.031221582297666e-4
allele num: 6598
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.57e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.243e1

DP
type: SiteQuality
SIO_000300: 1.568747e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-2

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 11

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 1974
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 10
allele frequency: 9.721952167995333e-4
allele num: 10286
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.667013347200555e-5
allele num: 11538
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65972
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.568747e6

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -3.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 2.57e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-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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variant carriers: 251

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515564851019975e-5
allele num: 65982
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

East Asian
type: Population
allele count: 252
allele frequency: 2.918693537178596e-2
allele num: 8634
num of homozygotes: 5

African
type: Population
allele count: 3
allele frequency: 2.91601866251944e-4
allele num: 10288
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211680600993578e-4
allele num: 16506
num of homozygotes: 1

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.34e-2

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

VQSLOD
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.579246e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.77e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

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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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65974
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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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: 894
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
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South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

MQRankSum
type: SiteQuality
SIO_000300: -6.09e-1

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

FS
type: SiteQuality
SIO_000300: 1.8703e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

QD
type: SiteQuality
SIO_000300: 1.083e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 38462
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1981
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3583
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 55
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9726
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3835
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 887
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 589
bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515472979116782e-5
allele num: 65986
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.38e0

VQSLOD
type: SiteQuality
SIO_000300: 6.28e-1

FS
type: SiteQuality
SIO_000300: 1.584e0

QD
type: SiteQuality
SIO_000300: 1.244e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

MQRankSum
type: SiteQuality
SIO_000300: 8.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.73e-1

DP
type: SiteQuality
SIO_000300: 1.573794e6

GenotypeQuality
all individuals: 891
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1983
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3579
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3840
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38472
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65984
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817300702689605e-4
allele num: 16508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.630000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.24e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
type: SiteQuality
SIO_000300: 2.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

FS
type: SiteQuality
SIO_000300: 2.618e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

DP
type: SiteQuality
SIO_000300: 1.57437e6

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3840
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 38472
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1983
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 8.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.031037827352085e-5
allele num: 65984
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

DP
type: SiteQuality
SIO_000300: 1.57437e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.69e-1

QD
type: SiteQuality
SIO_000300: 8.630000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: 2.84e-1

FS
type: SiteQuality
SIO_000300: 2.618e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.24e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.32e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3583
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 362
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38491
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3846
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9740
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65982
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.85e0

FS
type: SiteQuality
SIO_000300: 4.027e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e-1

MQ
type: SiteQuality
SIO_000300: 5.494e1

VQSLOD
type: SiteQuality
SIO_000300: -2.36e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

MQRankSum
type: SiteQuality
SIO_000300: -5.016e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.28e-1

DP
type: SiteQuality
SIO_000300: 1.574224e6

GenotypeQuality
all individuals: 51
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 56
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3507
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1879
bin: 9.75e1
variant carriers: 1008

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

GenotypeQuality
all individuals: 1948
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37882
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 698
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9587
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 51
allele frequency: 4.419410745233969e-3
allele num: 11540
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.060606060606061e-4
allele num: 6600
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

African
type: Population
allele count: 575
allele frequency: 5.583608467663624e-2
allele num: 10298
num of homozygotes: 19

European (Non-Finnish)
type: Population
allele count: 213
allele frequency: 3.227468331414025e-3
allele num: 65996
num of homozygotes: 0

South Asian
type: Population
allele count: 176
allele frequency: 1.066149745577902e-2
allele num: 16508
num of homozygotes: 1

Other
type: Population
allele count: 8
allele frequency: 8.948545861297539e-3
allele num: 894
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.468e1

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.82e0

FS
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 1.622249e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.398e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

GenotypeQuality
all individuals: 2001
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3543
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3790
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 37948
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66012
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e0

FS
type: SiteQuality
SIO_000300: 5.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-2

QD
type: SiteQuality
SIO_000300: 1.842e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.33e-2

DP
type: SiteQuality
SIO_000300: 1.605508e6

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3788
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37885
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2002
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9641
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1576
bin: 9.75e1
variant carriers: 4

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66004
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.116071428571429e-3
allele num: 896
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.526e0

FS
type: SiteQuality
SIO_000300: 3.189e0

VQSLOD
type: SiteQuality
SIO_000300: -5.979e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.847e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 1.605649e6

MQRankSum
type: SiteQuality
SIO_000300: 1.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.87e-1

GenotypeQuality
all individuals: 37907
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3794
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 621
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9650
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1576
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 66
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3545
bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.029752166272799e-5
allele num: 66012
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: 11542
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 1.606174e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.45e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.9e0

MQRankSum
type: SiteQuality
SIO_000300: -4.432e0

VQSLOD
type: SiteQuality
SIO_000300: -4.114e0

FS
type: SiteQuality
SIO_000300: 6.99e-1

MQ
type: SiteQuality
SIO_000300: 5.107e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-2

QD
type: SiteQuality
SIO_000300: 1.76e1

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37946
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3540
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 9651
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3794
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2000
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817300702689605e-4
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66022
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.594e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

VQSLOD
type: SiteQuality
SIO_000300: 9.409999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.957e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.21e-1

FS
type: SiteQuality
SIO_000300: 9.77e-1

QD
type: SiteQuality
SIO_000300: 1.5e1

DP
type: SiteQuality
SIO_000300: 1.606638e6

GenotypeQuality
all individuals: 3783
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3539
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1606
bin: 9.75e1
variant carriers: 29

GenotypeQuality
all individuals: 1995
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9636
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.120441051738762e-4
allele num: 66024
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.348214285714286e-3
allele num: 896
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 10
allele frequency: 8.664009703690869e-4
allele num: 11542
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.4e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

DP
type: SiteQuality
SIO_000300: 1.608034e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

VQSLOD
type: SiteQuality
SIO_000300: 4.06e0

QD
type: SiteQuality
SIO_000300: 1.324e1

GenotypeQuality
all individuals: 3785
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 88
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1600
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1999
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 57
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.732801940738174e-4
allele num: 11542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.120633766548517e-4
allele num: 66018
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e0

FS
type: SiteQuality
SIO_000300: 1.104e0

MQRankSum
type: SiteQuality
SIO_000300: -1.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

DP
type: SiteQuality
SIO_000300: 1.608581e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

QD
type: SiteQuality
SIO_000300: 1.434e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.5e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

GenotypeQuality
all individuals: 3792
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9661
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 38041
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2011
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3545
bin: 7.75e1
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: 11542
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66068
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.914e1

DP
type: SiteQuality
SIO_000300: 1.608693e6

QD
type: SiteQuality
SIO_000300: 1.697e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 1.1e0

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2011
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 626
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3543
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38056
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9670
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 743
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1595
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3792
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
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: 1.513317191283293e-5
allele num: 66080
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.659e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.14e-1

QD
type: SiteQuality
SIO_000300: 1.242e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.609174e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.566e0

MQRankSum
type: SiteQuality
SIO_000300: -1.308e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.42e-1

GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9672
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1602
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2010
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 628
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3544
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3791
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.078529278256922e-5
allele num: 66090
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
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: 11542
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.609522e6

VQSLOD
type: SiteQuality
SIO_000300: 7.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.433e0

FS
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

QD
type: SiteQuality
SIO_000300: 1.119e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.265e0

GenotypeQuality
all individuals: 38048
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 628
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3788
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1646
bin: 9.75e1
variant carriers: 47

GenotypeQuality
all individuals: 9669
bin: 6.75e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 47
allele frequency: 4.072084560734708e-3
allele num: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66104
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.19e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.769e0

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

MQRankSum
type: SiteQuality
SIO_000300: 1.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 5.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.17e-1

DP
type: SiteQuality
SIO_000300: 1.611491e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.24e-1

GenotypeQuality
all individuals: 327
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1615
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3557
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variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 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: 11542
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66118
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.610767e6

FS
type: SiteQuality
SIO_000300: 1.223e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.943e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.74e0

VQSLOD
type: SiteQuality
SIO_000300: 5.39e-1

QD
type: SiteQuality
SIO_000300: 1.28e1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

GenotypeQuality
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3553
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3788
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2011
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9676
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 7.5e0
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GenotypeQuality
all individuals: 38059
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1616
bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512310205069264e-5
allele num: 66124
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.56e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

FS
type: SiteQuality
SIO_000300: 2.912e0

DP
type: SiteQuality
SIO_000300: 1.610997e6

MQRankSum
type: SiteQuality
SIO_000300: -6.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.171e1

VQSLOD
type: SiteQuality
SIO_000300: 8.100000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.931e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.23e-1

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 745
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1616
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3552
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38091
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9669
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3785
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.023431594860166e-5
allele num: 66150
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 9.71e-1

FS
type: SiteQuality
SIO_000300: 8.55e-1

QD
type: SiteQuality
SIO_000300: 1.403e1

MQRankSum
type: SiteQuality
SIO_000300: -2.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 6.41e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.26e-1

DP
type: SiteQuality
SIO_000300: 1.611223e6