12-121614925-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121614925
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121614925
    reference: chr 12
allele count: 6
allele frequency: 4.990518015770037e-5
allele num: 120228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*426-25G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*660-25G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*59-25G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.973-25G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.703-25G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.106-25G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*376-25G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.973-25G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*728-25G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*728-25G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.706-25G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.463-25G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.706-25G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*513-25G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1058-25G>A
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23559
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13950
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

12-121614934-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121614934
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121614934
    reference: chr 12
allele count: 15368
allele frequency: 1.273640417032703e-1
allele num: 120662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*376-16C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.703-16C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.973-16C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.706-16C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1058-16C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*59-16C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.706-16C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.106-16C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*728-16C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.463-16C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*660-16C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*426-16C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*728-16C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.973-16C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*513-16C>T
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 5.75e1
  variant carriers: 947
genotype depth: GenotypeDepth
  all individuals: 12029
  bin: 2.75e1
  variant carriers: 914
genotype depth: GenotypeDepth
  all individuals: 18555
  bin: 2.25e1
  variant carriers: 477
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.75e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 4.25e1
  variant carriers: 2110
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.25e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.75e1
  variant carriers: 194
genotype quality: GenotypeQuality
num of homozygotes: 1548
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

12-121614940-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121614940
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121614941
    reference: chr 12
allele count: 1
allele frequency: 8.263370132874991e-6
allele num: 121016
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.463-9dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.703-9dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.106-9dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.706-9dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*59-9dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*513-9dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1058-9dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*426-9dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*376-9dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.973-9dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*660-9dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*728-9dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.973-9dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*728-9dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.706-9dupT
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1384
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

12-121614973-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121614973
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121614973
    reference: chr 12
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*82G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.729G>A
  hgvsp: ENST00000377162.2:c.729G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*751G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.486G>A
  hgvsp: ENST00000328963.5:c.486G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*399G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.726G>A
  hgvsp: ENST00000535250.1:c.726G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.996G>A
  hgvsp: ENST00000546057.1:c.996G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*751G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.129G>A
  hgvsp: ENST00000541446.1:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1081G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*536G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*683G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*449G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.996G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.729G>A
  hgvsp: ENST00000535600.1:c.729G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln332Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

12-121614973-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121614973
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121614973
    reference: chr 12
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*751G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*82G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*399G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.996G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.996G>C
  hgvsp: ENSP00000442349.1:p.Gln332His
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.486G>C
  hgvsp: ENSP00000330696.5:p.Gln162His
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.129G>C
  hgvsp: ENSP00000437471.1:p.Gln43His
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*683G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*751G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.726G>C
  hgvsp: ENSP00000442572.1:p.Gln242His
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*449G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1081G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.729G>C
  hgvsp: ENSP00000366367.2:p.Gln243His
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*536G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.729G>C
  hgvsp: ENSP00000442470.1:p.Gln243His
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln332His
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

12-121614974-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121614974
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121614974
    reference: chr 12
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.997C>T
  hgvsp: ENST00000546057.1:c.997C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*684C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.997C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*83C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*400C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*752C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.727C>T
  hgvsp: ENST00000535250.1:c.727C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.730C>T
  hgvsp: ENST00000377162.2:c.730C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*450C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.487C>T
  hgvsp: ENST00000328963.5:c.487C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.130C>T
  hgvsp: ENST00000541446.1:c.130C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.730C>T
  hgvsp: ENST00000535600.1:c.730C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1082C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*537C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*752C>T
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4984
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu333Leu
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

12-121614975-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121614975
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121614974
    reference: chr 12
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.733delG
  hgvsp: ENSP00000366367.2:p.Val245LeufsTer14
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*403delG
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*755delG
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.133delG
  hgvsp: ENSP00000437471.1:p.Val45LeufsTer65
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1085delG
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.730delG
  hgvsp: ENSP00000442572.1:p.Val244LeufsTer65
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*755delG
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.733delG
  hgvsp: ENSP00000442470.1:p.Val245LeufsTer14
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*540delG
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*687delG
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*453delG
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1000delG
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1000delG
  hgvsp: ENSP00000442349.1:p.Val334LeufsTer65
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.490delG
  hgvsp: ENSP00000330696.5:p.Val164LeufsTer65
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*86delG
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val334LeufsTer65
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: TG
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

12-121614977-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121614977
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121614976
    reference: chr 12
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.135delT
  hgvsp: ENSP00000437471.1:p.Val46CysfsTer64
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*542delT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*757delT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.492delT
  hgvsp: ENSP00000330696.5:p.Val165CysfsTer64
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.732delT
  hgvsp: ENSP00000442572.1:p.Val245CysfsTer64
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1002delT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*455delT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1002delT
  hgvsp: ENSP00000442349.1:p.Val335CysfsTer64
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.735delT
  hgvsp: ENSP00000442470.1:p.Val246CysfsTer13
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1087delT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.735delT
  hgvsp: ENSP00000366367.2:p.Val246CysfsTer13
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*405delT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*757delT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*689delT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*88delT
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val335CysfsTer64
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: GT
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

12-121614982-G-GCA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121614982
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121614984
    reference: chr 12
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: GCA
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*760_*761insCA
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1090_1091insCA
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*760_*761insCA
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*91_*92insCA
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1005_1006insCA
  hgvsp: ENSP00000442349.1:p.Tyr336HisfsTer64
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*408_*409insCA
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*545_*546insCA
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.738_739insCA
  hgvsp: ENSP00000442470.1:p.Tyr247HisfsTer13
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.738_739insCA
  hgvsp: ENSP00000366367.2:p.Tyr247HisfsTer13
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.735_736insCA
  hgvsp: ENSP00000442572.1:p.Tyr246HisfsTer64
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1005_1006insCA
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*458_*459insCA
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.138_139insCA
  hgvsp: ENSP00000437471.1:p.Tyr47HisfsTer64
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*692_*693insCA
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.495_496insCA
  hgvsp: ENSP00000330696.5:p.Tyr166HisfsTer64
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8774
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3651
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr336HisfsTer64
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

12-121614983-T-TATCCCACG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121614983
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121614991
    reference: chr 12
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: TATCCCACG
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.497_498insTCCCACGA
  hgvsp: ENSP00000330696.5:p.Ile167ProfsTer65
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsp: ENSP00000442349.1:p.Ile337ProfsTer65
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.740_741insTCCCACGA
  hgvsp: ENSP00000366367.2:p.Ile248ProfsTer14
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*93_*94insTCCCACGA
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.737_738insTCCCACGA
  hgvsp: ENSP00000442572.1:p.Ile247ProfsTer65
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.740_741insTCCCACGA
  hgvsp: ENSP00000442470.1:p.Ile248ProfsTer14
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.140_141insTCCCACGA
  hgvsp: ENSP00000437471.1:p.Ile48ProfsTer65
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile337ProfsTer65
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

12-121614985-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121614985
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121614985
    reference: chr 12
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1008C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.741C>T
  hgvsp: ENST00000377162.2:c.741C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*411C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.141C>T
  hgvsp: ENST00000541446.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*695C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*763C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*763C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1008C>T
  hgvsp: ENST00000546057.1:c.1008C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.498C>T
  hgvsp: ENST00000328963.5:c.498C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.738C>T
  hgvsp: ENST00000535250.1:c.738C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*461C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.741C>T
  hgvsp: ENST00000535600.1:c.741C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1093C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*548C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*94C>T
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8783
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr336Tyr
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: ClippingRankSum

12-121614988-C-CCTGTCCAAGAGCATGTTATCTATGTAAGACAGTGATAAGCAGGACTAGAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121614988
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615038
    reference: chr 12
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: CCTGTCCAAGAGCATGTTATCTATGTAAGACAGTGATAAGCAGGACTAGAA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsp: ENSP00000442470.1:p.Gly249LeufsTer9
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsp: ENSP00000442349.1:p.Gly338LeufsTer9
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsp: ENSP00000437471.1:p.Gly49LeufsTer9
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsp: ENSP00000442572.1:p.Gly248LeufsTer9
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsp: ENSP00000330696.5:p.Gly168LeufsTer9
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsp: ENSP00000366367.2:p.Gly249LeufsTer9
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: stop gained
filter: VQSRTrancheINDEL99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 2862
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly338LeufsTer9
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum

12-121615009-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615009
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615009
    reference: chr 12
allele count: 2
allele frequency: 1.647609318878308e-5
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*435C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*118C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*719C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1117C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.765C>T
  hgvsp: ENST00000535600.1:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.762C>T
  hgvsp: ENST00000535250.1:c.762C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.165C>T
  hgvsp: ENST00000541446.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*787C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.765C>T
  hgvsp: ENST00000377162.2:c.765C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*572C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*485C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1032C>T
  hgvsp: ENST00000546057.1:c.1032C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.522C>T
  hgvsp: ENST00000328963.5:c.522C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1032C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*787C>T
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe344Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

12-121615010-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615010
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615010
    reference: chr 12
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.166G>A
  hgvsp: ENSP00000437471.1:p.Gly56Ser
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1033G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.763G>A
  hgvsp: ENSP00000442572.1:p.Gly255Ser
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*119G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.766G>A
  hgvsp: ENSP00000366367.2:p.Gly256Ser
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*486G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.766G>A
  hgvsp: ENSP00000442470.1:p.Gly256Ser
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*720G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*573G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*436G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1033G>A
  hgvsp: ENSP00000442349.1:p.Gly345Ser
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*788G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.523G>A
  hgvsp: ENSP00000330696.5:p.Gly175Ser
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*788G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1118G>A
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4991
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly345Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

12-121615011-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615011
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615011
    reference: chr 12
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.524G>A
  hgvsp: ENSP00000330696.5:p.Gly175Asp
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1034G>A
  hgvsp: ENSP00000442349.1:p.Gly345Asp
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*120G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.767G>A
  hgvsp: ENSP00000366367.2:p.Gly256Asp
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*487G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.767G>A
  hgvsp: ENSP00000442470.1:p.Gly256Asp
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.764G>A
  hgvsp: ENSP00000442572.1:p.Gly255Asp
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*437G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.167G>A
  hgvsp: ENSP00000437471.1:p.Gly56Asp
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*789G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*721G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*574G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1034G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1119G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*789G>A
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly345Asp
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

12-121615012-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615012
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615012
    reference: chr 12
allele count: 0
allele frequency: 0.0e0
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*438T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*790T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1120T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1035T>C
  hgvsp: ENST00000546057.1:c.1035T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.168T>C
  hgvsp: ENST00000541446.1:c.168T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1035T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.768T>C
  hgvsp: ENST00000535600.1:c.768T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*575T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.768T>C
  hgvsp: ENST00000377162.2:c.768T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.765T>C
  hgvsp: ENST00000535250.1:c.765T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.525T>C
  hgvsp: ENST00000328963.5:c.525T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*790T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*121T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*722T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*488T>C
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gly345Gly
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

12-121615014-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615014
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615014
    reference: chr 12
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.170T>C
  hgvsp: ENSP00000437471.1:p.Leu57Pro
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*792T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*440T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1037T>C
  hgvsp: ENSP00000442349.1:p.Leu346Pro
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*724T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*123T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*792T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*490T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*577T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.527T>C
  hgvsp: ENSP00000330696.5:p.Leu176Pro
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.770T>C
  hgvsp: ENSP00000442470.1:p.Leu257Pro
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.770T>C
  hgvsp: ENSP00000366367.2:p.Leu257Pro
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1037T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1122T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.767T>C
  hgvsp: ENSP00000442572.1:p.Leu256Pro
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu346Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

12-121615022-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615022
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615022
    reference: chr 12
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.778G>A
  hgvsp: ENSP00000442470.1:p.Asp260Asn
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*800G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*793+7G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.528+7G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1130G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.171+7G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.768+7G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1038+7G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*124+7G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*491+7G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1045G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.778G>A
  hgvsp: ENSP00000366367.2:p.Asp260Asn
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*441+7G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*732G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*585G>A
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8807
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp260Asn
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

12-121615024-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615024
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615024
    reference: chr 12
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1132T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.768+9T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*441+9T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*491+9T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.780T>C
  hgvsp: ENST00000535600.1:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1047T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*734T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1038+9T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*587T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*124+9T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.171+9T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.780T>C
  hgvsp: ENST00000377162.2:c.780T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.528+9T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*793+9T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*802T>C
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18686
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp260Asp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum

12-121615028-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615028
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615029
    reference: chr 12
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1055dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.788dupT
  hgvsp: ENSP00000366367.2:p.His264ProfsTer12
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.788dupT
  hgvsp: ENSP00000442470.1:p.His264ProfsTer12
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*742dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*491+17dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*793+17dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*810dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.528+17dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.171+17dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*595dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1140dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*441+17dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1038+17dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*124+17dupT
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.768+17dupT
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His264ProfsTer12
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff

12-121615034-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615034
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615034
    reference: chr 12
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.768+19C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*744C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1057C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*793+19C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.790C>T
  hgvsp: ENSP00000366367.2:p.His264Tyr
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1038+19C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.528+19C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*597C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1142C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*812C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.790C>T
  hgvsp: ENSP00000442470.1:p.His264Tyr
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*491+19C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*441+19C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.171+19C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*124+19C>T
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2528
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His264Tyr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

12-121615036-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615036
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615036
    reference: chr 12
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1059T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1144T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.768+21T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1038+21T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.792T>C
  hgvsp: ENST00000535600.1:c.792T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*793+21T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*491+21T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*746T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.792T>C
  hgvsp: ENST00000377162.2:c.792T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.528+21T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*599T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*124+21T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*814T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*441+21T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.171+21T>C
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3652
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His264His
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ

12-121615040-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615040
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615040
    reference: chr 12
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*124+25T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.796T>G
  hgvsp: ENSP00000366367.2:p.Leu266Val
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.528+25T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*603T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1063T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*818T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*441+25T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*750T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1148T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.171+25T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*793+25T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.796T>G
  hgvsp: ENSP00000442470.1:p.Leu266Val
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1038+25T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.768+25T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*491+25T>G
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu266Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

12-121615043-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615043
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615043
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1066G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.799G>C
  hgvsp: ENSP00000442470.1:p.Gly267Arg
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1151G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.768+28G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*441+28G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*491+28G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*606G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*821G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1038+28G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.799G>C
  hgvsp: ENSP00000366367.2:p.Gly267Arg
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*753G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.528+28G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*793+28G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*124+28G>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.171+28G>C
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3656
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly267Arg
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

12-121615047-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615047
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615047
    reference: chr 12
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1070A>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1155A>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*610A>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1038+32A>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.803A>G
  hgvsp: ENSP00000442470.1:p.Lys268Arg
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*441+32A>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.528+32A>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*757A>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*491+32A>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*825A>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.171+32A>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.768+32A>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*793+32A>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.803A>G
  hgvsp: ENSP00000366367.2:p.Lys268Arg
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*124+32A>G
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys268Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

12-121615052-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615052
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615052
    reference: chr 12
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.808T>C
  hgvsp: ENSP00000442470.1:p.Phe270Leu
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*441+37T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1075T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*124+37T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1038+37T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*830T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*491+37T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*793+37T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*615T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*762T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.808T>C
  hgvsp: ENSP00000366367.2:p.Phe270Leu
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.528+37T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1160T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.171+37T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.768+37T>C
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18631
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe270Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

12-121615054-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615054
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615054
    reference: chr 12
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.810T>C
  hgvsp: ENST00000377162.2:c.810T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*832T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.171+39T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*124+39T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*793+39T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*491+39T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.810T>C
  hgvsp: ENST00000535600.1:c.810T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1077T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*441+39T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*764T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1038+39T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*617T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.528+39T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.768+39T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1162T>C
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18626
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe270Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

12-121615056-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615056
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615056
    reference: chr 12
allele count: 2
allele frequency: 1.647527884409444e-5
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.528+41G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.812G>A
  hgvsp: ENSP00000366367.2:p.Gly271Glu
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1079G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*124+41G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1038+41G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.768+41G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1164G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*766G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*441+41G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.812G>A
  hgvsp: ENSP00000442470.1:p.Gly271Glu
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*793+41G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.171+41G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*491+41G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*834G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*619G>A
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly271Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff

12-121615065-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615065
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615065
    reference: chr 12
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*843G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1088G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1173G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*492-35G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.529-35G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.821G>T
  hgvsp: ENSP00000442470.1:p.Ser274Ile
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*775G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*628G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000366367
  ensembl transcript: ENST00000377162
  gene symbol: P2RX7
  hgvsc: ENST00000377162.2:c.821G>T
  hgvsp: ENSP00000366367.2:p.Ser274Ile
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*442-35G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*125-35G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.172-35G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*794-35G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.769-35G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1039-35G>T
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2867
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8809
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser274Ile
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

12-121615074-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615074
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615074
    reference: chr 12
allele count: 3
allele frequency: 2.47137325974133e-5
allele num: 121390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*637G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.529-26G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*442-26G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.*2G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1182G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1039-26G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*852G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*784G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.172-26G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1097G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*794-26G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.769-26G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*125-26G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*492-26G>A
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

12-121615078-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615078
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615078
    reference: chr 12
allele count: 6
allele frequency: 4.942502224126001e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*125-22C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*794-22C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1186C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.172-22C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.529-22C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*788C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1101C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1039-22C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*641C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.*6C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*442-22C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*856C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*492-22C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.769-22C>T
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

12-121615079-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615079
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615079
    reference: chr 12
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*857G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.172-21G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1039-21G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.529-21G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*492-21G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*642G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.*7G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*789G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1102G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*125-21G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*442-21G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*794-21G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1187G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.769-21G>A
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5005
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1395
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2872
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

12-121615084-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615084
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615084
    reference: chr 12
allele count: 10
allele frequency: 8.237232289950576e-5
allele num: 121400
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*442-16T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.172-16T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*125-16T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1192T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1107T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.*12T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*862T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.529-16T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*647T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*794T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.769-16T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*794-16T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*492-16T>C
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1039-16T>C
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12548
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

12-121615090-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615090
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615090
    reference: chr 12
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1039-10T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.*18T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*794-10T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*868T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*125-10T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.172-10T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.529-10T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*800T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1113T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1198T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*653T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.769-10T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*442-10T>G
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*492-10T>G
  variant of: http://identifiers.org/hgnc/8537
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5011
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8822
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

12-121615102-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615102
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615102
    reference: chr 12
allele count: 7
allele frequency: 5.766062602965403e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1210C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*812C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1125C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*796C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*880C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*444C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.*30C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.771C>T
  hgvsp: ENST00000535250.1:c.771C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.531C>T
  hgvsp: ENST00000328963.5:c.531C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*494C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*127C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*665C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.174C>T
  hgvsp: ENST00000541446.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1041C>T
  hgvsp: ENST00000546057.1:c.1041C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1041C>T
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD

12-121615103-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615103
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615103
    reference: chr 12
allele count: 43464
allele frequency: 3.582060030658161e-1
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*881G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.175G>A
  hgvsp: ENSP00000437471.1:p.Ala59Thr
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*128G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*813G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*445G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.532G>A
  hgvsp: ENSP00000330696.5:p.Ala178Thr
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.*31G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*797G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.772G>A
  hgvsp: ENSP00000442572.1:p.Ala258Thr
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*666G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1042G>A
  hgvsp: ENSP00000442349.1:p.Ala348Thr
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*495G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1126G>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1211G>A
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 7.75e1
  variant carriers: 2452
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 6.75e1
  variant carriers: 3142
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 3.75e1
  variant carriers: 915
genotype depth: GenotypeDepth
  all individuals: 3084
  bin: 7.25e1
  variant carriers: 2841
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 5.25e1
  variant carriers: 2731
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 3.25e1
  variant carriers: 508
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 8.25e1
  variant carriers: 2049
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 5.75e1
  variant carriers: 3134
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 6.25e1
  variant carriers: 3268
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 8.75e1
  variant carriers: 1631
genotype quality: GenotypeQuality
hgvs: p.Ala348Thr
num of homozygotes: 8441
population: European (Finnish)
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum

12-121615103-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615103
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615103
    reference: chr 12
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1126G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.*31G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*813G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*881G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.175G>T
  hgvsp: ENSP00000437471.1:p.Ala59Ser
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*495G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.772G>T
  hgvsp: ENSP00000442572.1:p.Ala258Ser
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1042G>T
  hgvsp: ENSP00000442349.1:p.Ala348Ser
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*666G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*445G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*128G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.532G>T
  hgvsp: ENSP00000330696.5:p.Ala178Ser
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*797G>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1211G>T
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3084
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2624
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala348Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/12-121615111-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615111
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615111
    reference: chr 12
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*453C>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.540C>A
  hgvsp: ENSP00000330696.5:p.Phe180Leu
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1050C>A
  hgvsp: ENSP00000442349.1:p.Phe350Leu
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.780C>A
  hgvsp: ENSP00000442572.1:p.Phe260Leu
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*889C>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*136C>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*674C>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*821C>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.*39C>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.183C>A
  hgvsp: ENSP00000437471.1:p.Phe61Leu
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*805C>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*503C>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1219C>A
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1134C>A
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe350Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

12-121615114-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615114
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615114
    reference: chr 12
allele count: 4
allele frequency: 3.295110056675893e-5
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.543C>T
  hgvsp: ENST00000328963.5:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*824C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*139C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*677C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*456C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.*42C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*808C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*892C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.783C>T
  hgvsp: ENST00000535250.1:c.783C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*506C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.186C>T
  hgvsp: ENST00000541446.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1053C>T
  hgvsp: ENST00000546057.1:c.1053C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1222C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1137C>T
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3803
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7379
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile351Ile
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

12-121615117-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 121615117
    reference: chr 12
  end: Position
    type: ExactPosition
    position: 121615117
    reference: chr 12
allele count: 15
allele frequency: 1.235645913307083e-4
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442572
  ensembl transcript: ENST00000535250
  gene symbol: P2RX7
  hgvsc: ENST00000535250.1:c.786C>T
  hgvsp: ENST00000535250.1:c.786C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000439247
  ensembl transcript: ENST00000538011
  gene symbol: P2RX7
  hgvsc: ENST00000538011.1:c.*811C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000438586
  ensembl transcript: ENST00000537312
  gene symbol: P2RX7
  hgvsc: ENST00000537312.1:c.*827C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000443640
  ensembl transcript: ENST00000541564
  gene symbol: P2RX7
  hgvsc: ENST00000541564.1:c.*142C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437729
  ensembl transcript: ENST00000541716
  gene symbol: P2RX7
  hgvsc: ENST00000541716.1:c.*680C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000330696
  ensembl transcript: ENST00000328963
  gene symbol: P2RX7
  hgvsc: ENST00000328963.5:c.546C>T
  hgvsp: ENST00000328963.5:c.546C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442349
  ensembl transcript: ENST00000546057
  gene symbol: P2RX7
  hgvsc: ENST00000546057.1:c.1056C>T
  hgvsp: ENST00000546057.1:c.1056C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000445325
  ensembl transcript: ENST00000539606
  gene symbol: P2RX7
  hgvsc: ENST00000539606.1:c.*895C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000437471
  ensembl transcript: ENST00000541446
  gene symbol: P2RX7
  hgvsc: ENST00000541446.1:c.189C>T
  hgvsp: ENST00000541446.1:c.189C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000261826
  ensembl transcript: ENST00000261826
  gene symbol: P2RX7
  hgvsc: ENST00000261826.6:c.*509C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000441230
  ensembl transcript: ENST00000541022
  gene symbol: P2RX7
  hgvsc: ENST00000541022.1:c.*459C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000539695
  gene symbol: P2RX7
  hgvsc: ENST00000539695.1:n.1225C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000089041
  ensembl protein: ENSP00000442470
  ensembl transcript: ENST00000535600
  gene symbol: P2RX7
  hgvsc: ENST00000535600.1:c.*45C>T
  variant of: http://identifiers.org/hgnc/8537
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000089041
  ensembl transcript: ENST00000443520
  gene symbol: P2RX7
  hgvsc: ENST00000443520.3:n.1140C>T
  variant of: http://identifiers.org/hgnc/8537
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6397
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6152
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4940
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp352Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

16-555620-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 555620
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 555620
    reference: chr 16
allele count: 1
allele frequency: 1.339836004073102e-5
allele num: 74636
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.604G>C
  hgvsp: ENSP00000415919.1:p.Val202Leu
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1627G>C
  hgvsp: ENSP00000398730.1:p.Val543Leu
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1255G>C
  hgvsp: ENSP00000399644.1:p.Val419Leu
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.445G>C
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1492G>C
  hgvsp: ENSP00000262305.4:p.Val498Leu
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4264
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3020
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18969
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2588
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1075
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13782
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3191
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33324
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1107
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Val498Leu
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

16-555621-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 555621
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 555621
    reference: chr 16
allele count: 2
allele frequency: 2.68182793391976e-5
allele num: 74576
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.605T>A
  hgvsp: ENSP00000415919.1:p.Val202Glu
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1628T>A
  hgvsp: ENSP00000398730.1:p.Val543Glu
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.446T>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1493T>A
  hgvsp: ENSP00000262305.4:p.Val498Glu
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1256T>A
  hgvsp: ENSP00000399644.1:p.Val419Glu
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19018
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10708
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  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: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1046
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33493
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3200
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2102
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2577
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Val498Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

16-555632-G-GTTCAAGCTGTAGAACTGAGAAACGGGTTATGGGGGCCTAAGAGGAGCAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 555632
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 555681
    reference: chr 16
allele count: 1
allele frequency: 1.530549773478634e-5
allele num: 65336
alternate allele: GTTCAAGCTGTAGAACTGAGAAACGGGTTATGGGGGCCTAAGAGGAGCAC
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20990
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6486
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 925
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2804
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 837
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8115
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2094
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35080
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1317
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP

16-555637-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 555637
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 555637
    reference: chr 16
allele count: 1
allele frequency: 1.624800961882169e-5
allele num: 61546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1634+10G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.452+10G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1262+10G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.611+10G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1499+10G>A
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21023
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7571
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20955
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8278
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1972
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1172
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 747
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35085
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2806
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-555649-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 555649
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 555649
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 44558
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1499+22C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.452+22C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1262+22C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.611+22C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1634+22C>T
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16973
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14729
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20955
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  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 quality: GenotypeQuality
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3138
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1126
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16833
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26584
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2772
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2350
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2577
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

16-555650-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 555650
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 555650
    reference: chr 16
allele count: 5
allele frequency: 1.115872165684699e-4
allele num: 44808
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.611+23G>C
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1262+23G>C
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.452+23G>C
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1634+23G>C
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1499+23G>C
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14856
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21104
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16829
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27723
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2298
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17040
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1733
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2543
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3372
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.75e1
  variant carriers: 5
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: BaseQRankSum

16-555654-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 555654
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 555654
    reference: chr 16
allele count: 1
allele frequency: 2.640891564992342e-5
allele num: 37866
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.611+27C>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1634+27C>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1262+27C>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.452+27C>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1499+27C>G
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21691
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2520
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13969
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1925
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22373
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2394
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20393
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3541
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 778
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2799
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

16-555658-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 555658
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 555658
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 35238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1634+31G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.611+31G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1499+31G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1262+31G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.452+31G>A
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 22277
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12685
  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: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2362
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2115
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21080
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1898
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2618
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21374
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3983
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

16-555660-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 555660
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 555660
    reference: chr 16
allele count: 4
allele frequency: 1.205908953873983e-4
allele num: 33170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.452+33G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.611+33G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1499+33G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1262+33G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1634+33G>A
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22725
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11806
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
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 quality: GenotypeQuality
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2758
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1891
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21980
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2310
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19757
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4375
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1566
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD

16-555660-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 555660
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 555660
    reference: chr 16
allele count: 1
allele frequency: 3.014772384684956e-5
allele num: 33170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1634+33G>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.611+33G>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1499+33G>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1262+33G>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.452+33G>T
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11806
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18497
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1566
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2758
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2310
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19757
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4375
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21980
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1891
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

16-555664-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 555664
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 555664
    reference: chr 16
allele count: 3
allele frequency: 1.039429006998822e-4
allele num: 28862
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.611+37C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1634+37C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1499+37C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.452+37C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1262+37C>T
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9928
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23634
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  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: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2279
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5453
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22851
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16272
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3498
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 971
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2187
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1931
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1329
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-555665-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 555665
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 555665
    reference: chr 16
allele count: 3
allele frequency: 1.125281320330083e-4
allele num: 26660
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.452+38G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1634+38G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.611+38G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1262+38G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1499+38G>A
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9214
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24139
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1927
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4575
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2103
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3059
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1021
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6044
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13890
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22710
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

16-555678-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 555678
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 555678
    reference: chr 16
allele count: 3
allele frequency: 1.2636899747262e-4
allele num: 23740
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1262+51G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.452+51G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.611+51G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1634+51G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1499+51G>A
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8574
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25577
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12723
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3511
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6340
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1945
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 603
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

16-560632-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 560632
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 560632
    reference: chr 16
allele count: 2
allele frequency: 5.398693516169087e-5
allele num: 37046
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.453-28A>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000464263
  gene symbol: RAB11FIP3
  hgvsc: ENST00000464263.1:n.70A>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1263-28A>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.612-28A>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000461009
  gene symbol: RAB11FIP3
  hgvsc: ENST00000461009.1:n.180A>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1635-28A>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1500-28A>G
  variant of: http://identifiers.org/hgnc/17224
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10391
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30982
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10579
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4207
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3054
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4158
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4154
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3224
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8888
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

16-560634-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 560634
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 560634
    reference: chr 16
allele count: 1
allele frequency: 2.676372979338401e-5
allele num: 37364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.612-26C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1263-26C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1500-26C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000461009
  gene symbol: RAB11FIP3
  hgvsc: ENST00000461009.1:n.182C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000464263
  gene symbol: RAB11FIP3
  hgvsc: ENST00000464263.1:n.72C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.453-26C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1635-26C>T
  variant of: http://identifiers.org/hgnc/17224
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10593
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9786
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4570
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8510
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27084
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

16-560636-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 560636
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 560636
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 38002
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.612-24C>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.453-24C>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1500-24C>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000464263
  gene symbol: RAB11FIP3
  hgvsc: ENST00000464263.1:n.74C>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1635-24C>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000461009
  gene symbol: RAB11FIP3
  hgvsc: ENST00000461009.1:n.184C>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1263-24C>G
  variant of: http://identifiers.org/hgnc/17224
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9032
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31635
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4096
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28080
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2684
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2625
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

16-560644-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 560644
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 560644
    reference: chr 16
allele count: 1
allele frequency: 2.388458966274959e-5
allele num: 41868
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1500-16C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1263-16C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.453-16C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000464263
  gene symbol: RAB11FIP3
  hgvsc: ENST00000464263.1:n.82C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000461009
  gene symbol: RAB11FIP3
  hgvsc: ENST00000461009.1:n.192C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1635-16C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.612-16C>T
  variant of: http://identifiers.org/hgnc/17224
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1837
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9849
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6229
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3736
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30924
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1496
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP

16-560645-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 560645
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 560645
    reference: chr 16
allele count: 2
allele frequency: 4.703005220335794e-5
allele num: 42526
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000464263
  gene symbol: RAB11FIP3
  hgvsc: ENST00000464263.1:n.83C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1263-15C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000461009
  gene symbol: RAB11FIP3
  hgvsc: ENST00000461009.1:n.193C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.612-15C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1635-15C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1500-15C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.453-15C>T
  variant of: http://identifiers.org/hgnc/17224
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9814
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1527
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5951
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3888
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1437
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1700
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3689
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1581
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5530
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30746
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

16-560646-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 560646
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 560646
    reference: chr 16
allele count: 1
allele frequency: 2.315994256334244e-5
allele num: 43178
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1635-14C>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000461009
  gene symbol: RAB11FIP3
  hgvsc: ENST00000461009.1:n.194C>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1500-14C>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000464263
  gene symbol: RAB11FIP3
  hgvsc: ENST00000464263.1:n.84C>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1263-14C>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.453-14C>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.612-14C>G
  variant of: http://identifiers.org/hgnc/17224
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5654
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9812
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3661
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1341
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5305
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3862
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1694
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

16-560656-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 560656
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 560656
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 51280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000461009
  gene symbol: RAB11FIP3
  hgvsc: ENST00000461009.1:n.204C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1635-4C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.612-4C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1500-4C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1263-4C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.453-4C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000464263
  gene symbol: RAB11FIP3
  hgvsc: ENST00000464263.1:n.94C>T
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 12199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8605
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1741
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31017
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3045
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30660
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3159
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 5.25e1
  variant carriers: 0
hgvs: c.1500-4C>T
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum

16-560661-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 560661
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 560661
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 56388
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1264G>A
  hgvsp: ENSP00000399644.1:p.Ala422Thr
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1501G>A
  hgvsp: ENSP00000262305.4:p.Ala501Thr
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.613G>A
  hgvsp: ENSP00000415919.1:p.Ala205Thr
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000464263
  gene symbol: RAB11FIP3
  hgvsc: ENST00000464263.1:n.99G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000461009
  gene symbol: RAB11FIP3
  hgvsc: ENST00000461009.1:n.209G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1636G>A
  hgvsp: ENSP00000398730.1:p.Ala546Thr
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.454G>A
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29370
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8033
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2961
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1437
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala501Thr
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

16-560665-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 560665
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 560665
    reference: chr 16
allele count: 1
allele frequency: 1.640635253970337e-5
allele num: 60952
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000464263
  gene symbol: RAB11FIP3
  hgvsc: ENST00000464263.1:n.103A>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000461009
  gene symbol: RAB11FIP3
  hgvsc: ENST00000461009.1:n.213A>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1268A>G
  hgvsp: ENSP00000399644.1:p.Asn423Ser
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.617A>G
  hgvsp: ENSP00000415919.1:p.Asn206Ser
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.458A>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1640A>G
  hgvsp: ENSP00000398730.1:p.Asn547Ser
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1505A>G
  hgvsp: ENSP00000262305.4:p.Asn502Ser
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17141
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27787
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1749
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7344
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28063
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1766
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asn502Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

16-560667-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 560667
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 560667
    reference: chr 16
allele count: 4
allele frequency: 6.243171531137818e-5
allele num: 64070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.460G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1270G>A
  hgvsp: ENSP00000399644.1:p.Ala424Thr
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000461009
  gene symbol: RAB11FIP3
  hgvsc: ENST00000461009.1:n.215G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000464263
  gene symbol: RAB11FIP3
  hgvsc: ENST00000464263.1:n.105G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1507G>A
  hgvsp: ENSP00000262305.4:p.Ala503Thr
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.619G>A
  hgvsp: ENSP00000415919.1:p.Ala207Thr
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1642G>A
  hgvsp: ENSP00000398730.1:p.Ala548Thr
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18712
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7019
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1936
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3551
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1724
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1546
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18799
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26753
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala503Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

16-560692-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 560692
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 560692
    reference: chr 16
allele count: 1
allele frequency: 1.084363478638039e-5
allele num: 92220
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1295A>G
  hgvsp: ENSP00000399644.1:p.Gln432Arg
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1667A>G
  hgvsp: ENSP00000398730.1:p.Gln556Arg
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000461009
  gene symbol: RAB11FIP3
  hgvsc: ENST00000461009.1:n.240A>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.644A>G
  hgvsp: ENSP00000415919.1:p.Gln215Arg
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000464263
  gene symbol: RAB11FIP3
  hgvsc: ENST00000464263.1:n.130A>G
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1532A>G
  hgvsp: ENSP00000262305.4:p.Gln511Arg
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.485A>G
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13736
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1519
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14298
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln511Arg
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

16-560707-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 560707
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 560707
    reference: chr 16
allele count: 6
allele frequency: 5.718969822902568e-5
allele num: 104914
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000464263
  gene symbol: RAB11FIP3
  hgvsc: ENST00000464263.1:n.145G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1310G>A
  hgvsp: ENSP00000399644.1:p.Cys437Tyr
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.659G>A
  hgvsp: ENSP00000415919.1:p.Cys220Tyr
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1682G>A
  hgvsp: ENSP00000398730.1:p.Cys561Tyr
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.500G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1547G>A
  hgvsp: ENSP00000262305.4:p.Cys516Tyr
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000461009
  gene symbol: RAB11FIP3
  hgvsc: ENST00000461009.1:n.255G>A
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38718
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8048
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys516Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

16-560708-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 560708
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 560708
    reference: chr 16
allele count: 1
allele frequency: 9.462707469861277e-6
allele num: 105678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1311C>T
  hgvsp: ENST00000434585.1:c.1311C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.501C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1548C>T
  hgvsp: ENST00000262305.4:c.1548C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1683C>T
  hgvsp: ENST00000457159.1:c.1683C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.660C>T
  hgvsp: ENST00000450428.1:c.660C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000464263
  gene symbol: RAB11FIP3
  hgvsc: ENST00000464263.1:n.146C>T
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000461009
  gene symbol: RAB11FIP3
  hgvsc: ENST00000461009.1:n.256C>T
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8396
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7597
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 830
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3293
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Cys516Cys
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

16-560711-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 560711
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 560711
    reference: chr 16
allele count: 1
allele frequency: 9.215400777779826e-6
allele num: 108514
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.663G>A
  hgvsp: ENST00000450428.1:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1314G>A
  hgvsp: ENST00000434585.1:c.1314G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1686G>A
  hgvsp: ENST00000457159.1:c.1686G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000464263
  gene symbol: RAB11FIP3
  hgvsc: ENST00000464263.1:n.149G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000461009
  gene symbol: RAB11FIP3
  hgvsc: ENST00000461009.1:n.259G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1551G>A
  hgvsp: ENST00000262305.4:c.1551G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.504G>A
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  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: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.25e1
  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 quality: GenotypeQuality
  all individuals: 284
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6268
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 795
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43826
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu517Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

16-560715-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 560715
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 560715
    reference: chr 16
allele count: 17
allele frequency: 1.541726370776123e-4
allele num: 110266
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000461009
  gene symbol: RAB11FIP3
  hgvsc: ENST00000461009.1:n.263G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000399644
  ensembl transcript: ENST00000434585
  gene symbol: RAB11FIP3
  hgvsc: ENST00000434585.1:c.1318G>A
  hgvsp: ENSP00000399644.1:p.Val440Ile
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000262305
  ensembl transcript: ENST00000262305
  gene symbol: RAB11FIP3
  hgvsc: ENST00000262305.4:c.1555G>A
  hgvsp: ENSP00000262305.4:p.Val519Ile
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000487899
  gene symbol: RAB11FIP3
  hgvsc: ENST00000487899.1:n.508G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000090565
  ensembl transcript: ENST00000464263
  gene symbol: RAB11FIP3
  hgvsc: ENST00000464263.1:n.153G>A
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000415919
  ensembl transcript: ENST00000450428
  gene symbol: RAB11FIP3
  hgvsc: ENST00000450428.1:c.667G>A
  hgvsp: ENSP00000415919.1:p.Val223Ile
  variant of: http://identifiers.org/hgnc/17224
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000090565
  ensembl protein: ENSP00000398730
  ensembl transcript: ENST00000457159
  gene symbol: RAB11FIP3
  hgvsc: ENST00000457159.1:c.1690G>A
  hgvsp: ENSP00000398730.1:p.Val564Ile
  variant of: http://identifiers.org/hgnc/17224
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41280
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5008
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9174
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 3
hgvs: p.Val519Ile
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 1838
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 8628
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 174
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 216
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 342
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 299
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3706
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2241
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 178
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11131
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 254
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 236
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 565
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1867
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7617
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4150
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3615
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2481
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21420
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5263
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
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: 6574
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.56956429587913e-5
allele num: 66054
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.751969193068441e-5
allele num: 11426
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.13e0

FS
type: SiteQuality
SIO_000300: 8.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.47e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.41e-2

DP
type: SiteQuality
SIO_000300: 1.999551e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.461e0

QD
type: SiteQuality
SIO_000300: 1.461e1

GenotypeDepth
all individuals: 454
bin: 7.25e1
variant carriers: 212

GenotypeDepth
all individuals: 1910
bin: 5.25e1
variant carriers: 1324

GenotypeDepth
all individuals: 8455
bin: 3.25e1
variant carriers: 1575

GenotypeDepth
all individuals: 290
bin: 8.25e1
variant carriers: 116

GenotypeDepth
all individuals: 2601
bin: 9.75e1
variant carriers: 849

GenotypeDepth
all individuals: 4924
bin: 3.75e1
variant carriers: 1935

GenotypeDepth
all individuals: 2804
bin: 4.75e1
variant carriers: 1879

GenotypeDepth
all individuals: 940
bin: 6.25e1
variant carriers: 607

GenotypeDepth
all individuals: 638
bin: 6.75e1
variant carriers: 341

GenotypeDepth
all individuals: 373
bin: 1.75e1
variant carriers: 171

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 6

GenotypeQuality
all individuals: 202
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 8

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

GenotypeQuality
all individuals: 2854
bin: 7.25e1
variant carriers: 31

GenotypeQuality
all individuals: 17082
bin: 6.25e1
variant carriers: 23

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 8

GenotypeQuality
all individuals: 241
bin: 3.75e1
variant carriers: 14

GenotypeQuality
all individuals: 258
bin: 3.25e1
variant carriers: 10

GenotypeQuality
all individuals: 6011
bin: 6.75e1
variant carriers: 37

GenotypeQuality
all individuals: 4106
bin: 7.75e1
variant carriers: 42

GenotypeQuality
all individuals: 121
bin: 4.25e1
variant carriers: 13

GenotypeQuality
all individuals: 22258
bin: 9.75e1
variant carriers: 13435

GenotypeQuality
all individuals: 329
bin: 2.25e1
variant carriers: 7

GenotypeQuality
all individuals: 3275
bin: 8.25e1
variant carriers: 57

GenotypeQuality
all individuals: 170
bin: 5.25e1
variant carriers: 22

GenotypeQuality
all individuals: 1471
bin: 8.75e1
variant carriers: 33

GenotypeQuality
all individuals: 1961
bin: 9.25e1
variant carriers: 67

GenotypeQuality
all individuals: 136
bin: 4.75e1
variant carriers: 15

GenotypeQuality
all individuals: 141
bin: 5.75e1
variant carriers: 15

South Asian
type: Population
allele count: 2603
allele frequency: 1.583718666342176e-1
allele num: 16436
num of homozygotes: 241

African
type: Population
allele count: 1037
allele frequency: 1.00426108851443e-1
allele num: 10326
num of homozygotes: 48

East Asian
type: Population
allele count: 1433
allele frequency: 1.665117359981408e-1
allele num: 8606
num of homozygotes: 123

European (Non-Finnish)
type: Population
allele count: 5126
allele frequency: 7.726395755456408e-2
allele num: 66344
num of homozygotes: 201

Latino
type: Population
allele count: 4299
allele frequency: 3.750654336067004e-1
allele num: 11462
num of homozygotes: 883

Other
type: Population
allele count: 106
allele frequency: 1.177777777777778e-1
allele num: 900
num of homozygotes: 5

European (Finnish)
type: Population
allele count: 764
allele frequency: 1.159684274438373e-1
allele num: 6588
num of homozygotes: 47

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.290000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.08e-1

QD
type: SiteQuality
SIO_000300: 1.571e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.347e0

FS
type: SiteQuality
SIO_000300: 7.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.89e0

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

DP
type: SiteQuality
SIO_000300: 2.286594e6

GenotypeDepth
all individuals: 234
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 692
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12172
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2851
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 485
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4935
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 388
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3931
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6543
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18772
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17889
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4675
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2696
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3260
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1952
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503126503126503e-5
allele num: 66528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.761e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

DP
type: SiteQuality
SIO_000300: 2.270731e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.96e-1

QD
type: SiteQuality
SIO_000300: 1.415e1

FS
type: SiteQuality
SIO_000300: 4.199e0

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

MQ
type: SiteQuality
SIO_000300: 6.017e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.92e-1

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 332
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8761
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1393
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2529
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2860
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3651
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 944
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 487
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4983
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4004
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1998
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18272
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3346
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2736
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18832
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4752
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6666
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

VQSLOD
type: SiteQuality
SIO_000300: 3.13e-1

DP
type: SiteQuality
SIO_000300: 2.283151e6

FS
type: SiteQuality
SIO_000300: 6.435e0

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

MQ
type: SiteQuality
SIO_000300: 5.909e1

QD
type: SiteQuality
SIO_000300: 1.074e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.705e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

GenotypeDepth
all individuals: 1951
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4983
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18791
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2860
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 3651
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8761
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 332
bin: 8.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4752
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18832
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3346
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18272
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4004
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2736
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6666
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.074e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.705e0

FS
type: SiteQuality
SIO_000300: 6.435e0

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

MQ
type: SiteQuality
SIO_000300: 5.909e1

VQSLOD
type: SiteQuality
SIO_000300: 3.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

DP
type: SiteQuality
SIO_000300: 2.283151e6

GenotypeDepth
all individuals: 3650
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2529
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18791
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 944
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1394
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2860
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 7.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 486
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6664
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18278
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3347
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18833
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4756
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4003
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2736
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2000
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.386e0

MQRankSum
type: SiteQuality
SIO_000300: 8.98e-1

DP
type: SiteQuality
SIO_000300: 2.28324e6

MQ
type: SiteQuality
SIO_000300: 5.855e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.900000000000001e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.271e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

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

GenotypeDepth
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12425
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18791
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3651
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 694
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1393
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2529
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18833
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2736
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2000
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6667
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18288
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3346
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4004
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4756
bin: 7.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -6.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.26e0

DP
type: SiteQuality
SIO_000300: 2.283389e6

MQ
type: SiteQuality
SIO_000300: 6.021e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.04e-1

FS
type: SiteQuality
SIO_000300: 1.103e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

QD
type: SiteQuality
SIO_000300: 1.454e1

GenotypeDepth
all individuals: 694
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1394
bin: 5.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 18
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1952
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12432
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4982
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 944
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18833
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3344
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2001
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6670
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18280
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2737
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4005
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4757
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.45e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.08e-1

FS
type: SiteQuality
SIO_000300: 1.048e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.998e1

MQRankSum
type: SiteQuality
SIO_000300: 5.45e-1

QD
type: SiteQuality
SIO_000300: 1.751e1

VQSLOD
type: SiteQuality
SIO_000300: 3.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.681e0

DP
type: SiteQuality
SIO_000300: 2.283562e6

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

GenotypeDepth
all individuals: 2861
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 18777
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1394
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2528
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 388
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1952
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4983
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2001
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2739
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18278
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4762
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4006
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3348
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6672
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18835
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 8.5054e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.376e1

MQRankSum
type: SiteQuality
SIO_000300: -1.028e1

MQ
type: SiteQuality
SIO_000300: 5.574e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.245e0

QD
type: SiteQuality
SIO_000300: 3.22e0

DP
type: SiteQuality
SIO_000300: 2.283575e6

GenotypeDepth
all individuals: 8776
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4983
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 945
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2861
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 694
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3651
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6675
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4764
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18835
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4008
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2001
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2739
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3350
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18274
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.2e0

VQSLOD
type: SiteQuality
SIO_000300: -1.415e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.28e0

FS
type: SiteQuality
SIO_000300: 8.553400000000001e1

MQRankSum
type: SiteQuality
SIO_000300: -1.015e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.366e0

MQ
type: SiteQuality
SIO_000300: 5.584e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.98e0

DP
type: SiteQuality
SIO_000300: 2.283606e6

GenotypeDepth
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3652
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 331
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4984
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12454
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2862
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2528
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6681
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2001
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3355
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4007
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4764
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18256
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18834
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2739
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.649e0

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

MQRankSum
type: SiteQuality
SIO_000300: -2.477e0

DP
type: SiteQuality
SIO_000300: 2.283735e6

MQ
type: SiteQuality
SIO_000300: 5.578e1

QD
type: SiteQuality
SIO_000300: 1.575e1

FS
type: SiteQuality
SIO_000300: 3.587e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.472e0

GenotypeDepth
all individuals: 3650
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8787
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18745
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2528
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 694
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6686
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4009
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3355
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4762
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2739
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18245
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18835
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2001
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.7375e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.23e0

MQRankSum
type: SiteQuality
SIO_000300: -7.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.999e0

QD
type: SiteQuality
SIO_000300: 2.1e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.573e0

DP
type: SiteQuality
SIO_000300: 2.283856e6

MQ
type: SiteQuality
SIO_000300: 5.782e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e0

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

GenotypeDepth
all individuals: 695
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 486
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8804
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2864
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1394
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4987
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6684
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18840
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 18253
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2004
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3353
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2741
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4013
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4772
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 66728
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 2.284555e6

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-1

QD
type: SiteQuality
SIO_000300: 1.12e1

MQRankSum
type: SiteQuality
SIO_000300: 4.87e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.87e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e-1

GenotypeDepth
all individuals: 3652
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8804
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 18708
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 486
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12484
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2863
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 695
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18841
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3354
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2740
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6684
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18249
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4773
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4014
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2003
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.14e-1

FS
type: SiteQuality
SIO_000300: 1.1024e1

VQSLOD
type: SiteQuality
SIO_000300: -1.811e0

QD
type: SiteQuality
SIO_000300: 7.17e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.55e0

DP
type: SiteQuality
SIO_000300: 2.284571e6

GenotypeDepth
all individuals: 1394
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4988
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1952
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2529
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 12483
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2864
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 695
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 946
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18841
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3356
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6685
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4014
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4775
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2740
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18256
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.115e0

MQRankSum
type: SiteQuality
SIO_000300: 1.99e0

QD
type: SiteQuality
SIO_000300: 1.088e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.757e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.284635e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e0

VQSLOD
type: SiteQuality
SIO_000300: -1.994e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 18709
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4988
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12485
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3652
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1394
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 487
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 695
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6686
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2741
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4014
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18257
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4774
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18843
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3356
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2003
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 4.611e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.942e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.02e0

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

DP
type: SiteQuality
SIO_000300: 2.284594e6

VQSLOD
type: SiteQuality
SIO_000300: 2.29e-1

QD
type: SiteQuality
SIO_000300: 1.197e1

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

GenotypeDepth
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12493
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18701
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1952
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8802
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 695
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4987
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1394
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18252
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3355
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6686
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2003
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4774
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18842
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4013
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2741
bin: 9.25e1
variant carriers: 0

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

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.1e-2

MQ
type: SiteQuality
SIO_000300: 5.853e1

DP
type: SiteQuality
SIO_000300: 2.284633e6

MQRankSum
type: SiteQuality
SIO_000300: 6.32e-1

FS
type: SiteQuality
SIO_000300: 1.363e0

VQSLOD
type: SiteQuality
SIO_000300: -9.069e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.259e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.137e1

GenotypeDepth
all individuals: 1953
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 486
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 695
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12498
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2529
bin: 9.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 331
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 945
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2863
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4775
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3357
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6687
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18842
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 18249
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2003
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4014
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2741
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.284556e6

FS
type: SiteQuality
SIO_000300: 4.7e-1

QD
type: SiteQuality
SIO_000300: 1.323e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.464e0

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

MQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-1

GenotypeDepth
all individuals: 331
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2864
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 945
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12502
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1395
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 695
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3651
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1953
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18245
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6689
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3359
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4775
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2004
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4015
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2741
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18843
bin: 9.75e1
variant carriers: 2

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -5.943000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-1

FS
type: SiteQuality
SIO_000300: 8.827e0

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.284623e6

QD
type: SiteQuality
SIO_000300: 1.441e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.8e-2

GenotypeDepth
all individuals: 3653
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 224
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4990
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 387
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 331
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 487
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2865
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 945
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 18666
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4016
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6684
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3360
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2004
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18843
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2741
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4774
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18202
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.88e0

MQRankSum
type: SiteQuality
SIO_000300: 8.92e-1

DP
type: SiteQuality
SIO_000300: 2.284719e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.69e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

QD
type: SiteQuality
SIO_000300: 7.65e0

FS
type: SiteQuality
SIO_000300: 2.704e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8810
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4990
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 387
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1953
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3653
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2865
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1394
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18842
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4016
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6684
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2741
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4774
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18225
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3361
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.839e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.517e0

MQ
type: SiteQuality
SIO_000300: 5.915e1

VQSLOD
type: SiteQuality
SIO_000300: -2.562e0

MQRankSum
type: SiteQuality
SIO_000300: -1.787e0

DP
type: SiteQuality
SIO_000300: 2.284726e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e0

QD
type: SiteQuality
SIO_000300: 1.008e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e-2

GenotypeDepth
all individuals: 387
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 487
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4989
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18662
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12514
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2865
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2529
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 695
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6684
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3364
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18215
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18842
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2741
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4016
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4775
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

QD
type: SiteQuality
SIO_000300: 1.34e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e0

VQSLOD
type: SiteQuality
SIO_000300: -3.309e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.71e-1

FS
type: SiteQuality
SIO_000300: 7.062e0

DP
type: SiteQuality
SIO_000300: 2.284746e6

MQ
type: SiteQuality
SIO_000300: 5.905e1

GenotypeDepth
all individuals: 1394
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2865
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 224
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 387
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8805
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2530
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 488
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 945
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6681
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18221
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3366
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4016
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2741
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18843
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2005
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4774
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.965e0

MQRankSum
type: SiteQuality
SIO_000300: -1.65e-1

DP
type: SiteQuality
SIO_000300: 2.284809e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.64e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

QD
type: SiteQuality
SIO_000300: 1.427e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.5e-2

GenotypeDepth
all individuals: 695
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 487
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4990
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1953
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12513
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1394
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 945
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8807
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2006
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4017
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2742
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18209
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4776
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3366
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6679
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18842
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.28493e6

VQSLOD
type: SiteQuality
SIO_000300: 3.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 1.854e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.466e0

QD
type: SiteQuality
SIO_000300: 1.37e1

GenotypeDepth
all individuals: 8806
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 387
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 696
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18642
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4993
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12518
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1394
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1953
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6682
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4019
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3367
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2743
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4771
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18843
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18206
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.285007e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.85e0

FS
type: SiteQuality
SIO_000300: 1.297e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 1.19e1

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

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

GenotypeDepth
all individuals: 3655
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 696
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1394
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2866
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 387
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2530
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 4771
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18843
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4018
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18202
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2743
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6686
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3368
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.365e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.0e-3

QD
type: SiteQuality
SIO_000300: 1.212e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.768e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.3e-2

DP
type: SiteQuality
SIO_000300: 2.285046e6

MQ
type: SiteQuality
SIO_000300: 5.983e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

VQSLOD
type: SiteQuality
SIO_000300: -4.464e-1

GenotypeDepth
all individuals: 8808
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3655
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 945
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1953
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1394
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 487
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 332
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 696
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2530
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18197
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4018
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18845
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2005
bin: 8.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2743
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6686
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3369
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4772
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e0

DP
type: SiteQuality
SIO_000300: 2.285111e6

QD
type: SiteQuality
SIO_000300: 1.498e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 2866
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 2532
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 8810
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 331
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1394
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4994
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 945
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6683
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18185
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3369
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4018
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18846
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4773
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2743
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.358e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.937e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: 4.12e-1

FS
type: SiteQuality
SIO_000300: 2.709e0

DP
type: SiteQuality
SIO_000300: 2.285352e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.04e-2

GenotypeDepth
all individuals: 388
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1394
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3655
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4996
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 696
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 18593
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1954
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 330
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2004
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4020
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18166
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18847
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 6693
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2744
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3369
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4771
bin: 7.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.04e-2

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.364e0

VQSLOD
type: SiteQuality
SIO_000300: 8.76e-1

FS
type: SiteQuality
SIO_000300: 2.995e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

DP
type: SiteQuality
SIO_000300: 2.28529e6

MQRankSum
type: SiteQuality
SIO_000300: 1.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.37e-1

QD
type: SiteQuality
SIO_000300: 1.289e1

GenotypeDepth
all individuals: 224
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2868
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2533
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 946
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 487
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1954
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6686
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18850
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18126
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2006
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2743
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3374
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4772
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4019
bin: 8.25e1
variant carriers: 1

East Asian
type: Population
allele count: 2
allele frequency: 2.31107002542177e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66730
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -5.55e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.98e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.05e-2

DP
type: SiteQuality
SIO_000300: 2.28581e6

FS
type: SiteQuality
SIO_000300: 6.668e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.91e0

QD
type: SiteQuality
SIO_000300: 1.01e1

GenotypeDepth
all individuals: 697
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1955
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5001
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2536
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 948
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 330
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3374
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4021
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4771
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18855
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18114
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6685
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2744
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.49243264303054e-5
allele num: 66734
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.286288e6

QD
type: SiteQuality
SIO_000300: 1.313e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

FS
type: SiteQuality
SIO_000300: 5.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.25e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

GenotypeDepth
all individuals: 1955
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3655
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 947
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2534
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4024
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18115
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18854
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6688
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4772
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2744
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3377
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 3.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-1

DP
type: SiteQuality
SIO_000300: 2.286147e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.08e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

MQ
type: SiteQuality
SIO_000300: 5.949e1

QD
type: SiteQuality
SIO_000300: 1.206e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.3e-2

GenotypeDepth
all individuals: 8821
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3659
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2536
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 5005
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 699
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 332
bin: 8.25e1
variant carriers: 2

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

GenotypeQuality
all individuals: 2006
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4020
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 18088
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3376
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18870
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 6688
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4777
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2742
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.498441620714457e-4
allele num: 66736
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

QD
type: SiteQuality
SIO_000300: 1.438e1

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.103e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.07e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

DP
type: SiteQuality
SIO_000300: 2.286562e6

GenotypeDepth
all individuals: 2872
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 388
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 18512
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1399
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12535
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2534
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18084
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6691
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3379
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4778
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4024
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2008
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18870
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2744
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996883241428914e-5
allele num: 66736
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: 11570
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.41e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-1

FS
type: SiteQuality
SIO_000300: 6.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

QD
type: SiteQuality
SIO_000300: 1.356e1

MQ
type: SiteQuality
SIO_000300: 5.971e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.96e-1

DP
type: SiteQuality
SIO_000300: 2.286695e6

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

GenotypeDepth
all individuals: 8838
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1964
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1409
bin: 5.75e1
variant carriers: 3

GenotypeDepth
all individuals: 330
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12545
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 952
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3661
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 490
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 224
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4029
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3385
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2750
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4786
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6689
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17993
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2006
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18897
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.04890913450012e-4
allele num: 66736
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.333e0

DP
type: SiteQuality
SIO_000300: 2.288091e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.73e0

FS
type: SiteQuality
SIO_000300: 2.476e0

QD
type: SiteQuality
SIO_000300: 1.065e1

GenotypeDepth
all individuals: 3318
bin: 4.25e1
variant carriers: 1431

GenotypeDepth
all individuals: 5322
bin: 2.75e1
variant carriers: 255

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

GenotypeDepth
all individuals: 6971
bin: 2.25e1
variant carriers: 89

GenotypeDepth
all individuals: 59
bin: 1.75e1
variant carriers: 37

GenotypeDepth
all individuals: 3795
bin: 4.75e1
variant carriers: 2140

GenotypeDepth
all individuals: 7635
bin: 9.75e1
variant carriers: 7068

GenotypeDepth
all individuals: 1412
bin: 9.25e1
variant carriers: 1331

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 5

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 6

GenotypeQuality
all individuals: 2742
bin: 6.75e1
variant carriers: 24

GenotypeQuality
all individuals: 1819
bin: 7.75e1
variant carriers: 31

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 7

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 8.25e1
variant carriers: 29

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 803
bin: 8.75e1
variant carriers: 31

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 4

GenotypeQuality
all individuals: 43449
bin: 9.75e1
variant carriers: 34790

GenotypeQuality
all individuals: 7518
bin: 6.25e1
variant carriers: 5

GenotypeQuality
all individuals: 1395
bin: 7.25e1
variant carriers: 19

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 12

GenotypeQuality
all individuals: 1143
bin: 9.25e1
variant carriers: 54

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 4

European (Finnish)
type: Population
allele count: 2995
allele frequency: 4.532384987893462e-1
allele num: 6608
num of homozygotes: 667

African
type: Population
allele count: 4744
allele frequency: 4.558908322121853e-1
allele num: 10406
num of homozygotes: 1076

Other
type: Population
allele count: 346
allele frequency: 3.81057268722467e-1
allele num: 908
num of homozygotes: 65

South Asian
type: Population
allele count: 6495
allele frequency: 3.934932751726645e-1
allele num: 16506
num of homozygotes: 1313

Latino
type: Population
allele count: 1854
allele frequency: 1.602974234826215e-1
allele num: 11566
num of homozygotes: 175

European (Non-Finnish)
type: Population
allele count: 26065
allele frequency: 3.90756176541137e-1
allele num: 66704
num of homozygotes: 5088

East Asian
type: Population
allele count: 965
allele frequency: 1.116898148148148e-1
allele num: 8640
num of homozygotes: 57

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.33e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.22e-1

QD
type: SiteQuality
SIO_000300: 1.906e1

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.68582e6

VQSLOD
type: SiteQuality
SIO_000300: 5.95e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

GenotypeDepth
all individuals: 7635
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4055
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5322
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6971
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3260
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3804
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3318
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7518
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2742
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 3.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1819
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43449
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1395
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 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: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
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: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.35e-1

QD
type: SiteQuality
SIO_000300: 1.906e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.15e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 5.95e0

MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

DP
type: SiteQuality
SIO_000300: 3.68582e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.33e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.22e-1

GenotypeDepth
all individuals: 2680
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4936
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 6399
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1010
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6355
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2297
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6153
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4423
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3057
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 19
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3570
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3419
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31835
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9809
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.947e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

DP
type: SiteQuality
SIO_000300: 2.772023e6

QD
type: SiteQuality
SIO_000300: 3.025e1

VQSLOD
type: SiteQuality
SIO_000300: -5.69e-2

FS
type: SiteQuality
SIO_000300: 2.174e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.27e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

GenotypeDepth
all individuals: 494
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2678
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1320
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 610
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6154
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6399
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2297
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6352
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4420
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3057
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3566
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9810
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3418
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31833
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 3
allele frequency: 2.882952142994427e-4
allele num: 10406
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: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.771926e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 9.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

QD
type: SiteQuality
SIO_000300: 1.402e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.0e-3

GenotypeDepth
all individuals: 6348
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2680
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2298
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 494
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 611
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1318
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 789
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3804
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3563
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4425
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31838
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3417
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2405
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3055
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9802
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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: 15
allele frequency: 1.733302519066328e-3
allele num: 8654
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.92e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.13e0

DP
type: SiteQuality
SIO_000300: 2.772028e6

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: 2.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e-1

FS
type: SiteQuality
SIO_000300: 1.751e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.1e-2

QD
type: SiteQuality
SIO_000300: 1.189e1

GenotypeQuality
all individuals: 324
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2129
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6002
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41286
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.463100880162491e-5
allele num: 11816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 530
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2964
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.999999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 8.0634e5

QD
type: SiteQuality
SIO_000300: 3.321e1

VQSLOD
type: SiteQuality
SIO_000300: -2.887e0

MQRankSum
type: SiteQuality
SIO_000300: 8.090000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.66e0

GenotypeQuality
all individuals: 42
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13969
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.848014737964803e-5
allele num: 41254
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5994
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11810
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2938
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5466
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.67e-1

DP
type: SiteQuality
SIO_000300: 8.04748e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-1

QD
type: SiteQuality
SIO_000300: 1.025e1

GenotypeQuality
all individuals: 149
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35846
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2508
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.71291538198013e-4
allele num: 5838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4952
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11078
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4660
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.53e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.66e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.87e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.5e-1

DP
type: SiteQuality
SIO_000300: 6.98262e5

GenotypeQuality
all individuals: 185
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6864
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4368
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2328
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33616
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.805706031058144e-4
allele num: 5538
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10774
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

QD
type: SiteQuality
SIO_000300: 8.220000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.0e0

MQ
type: SiteQuality
SIO_000300: 5.705e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.233e0

DP
type: SiteQuality
SIO_000300: 6.6179e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.84e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.42e-1

GenotypeQuality
all individuals: 402
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1879
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 653
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23184
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4264
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2682
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 308
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1338
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.393e0

VQSLOD
type: SiteQuality
SIO_000300: 7.74e-1

DP
type: SiteQuality
SIO_000300: 5.37771e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 1.372e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.35e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.29e-1

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1799
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3144
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9672
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1402
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 296
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4290
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2724
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 2.147766323024055e-4
allele num: 23280
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 1.943e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.88e-2

QD
type: SiteQuality
SIO_000300: 1.368e1

DP
type: SiteQuality
SIO_000300: 5.35201e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.818e0

GenotypeQuality
all individuals: 2257
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 73
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2026
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.089561996077577e-4
allele num: 9178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1016
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3784
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19006
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 284
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.36e-1

DP
type: SiteQuality
SIO_000300: 4.8534e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.86e-2

QD
type: SiteQuality
SIO_000300: 6.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.073e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.54e-1

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 278
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3538
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2358
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1800
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.159e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.219e0

DP
type: SiteQuality
SIO_000300: 4.68838e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.014e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.04e-2

QD
type: SiteQuality
SIO_000300: 4.96e0

GenotypeQuality
all individuals: 16
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 63
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1906
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 1.359927470534905e-3
allele num: 2206
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8860
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.219679064560268e-5
allele num: 16078
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.034e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

FS
type: SiteQuality
SIO_000300: 2.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.66e-2

QD
type: SiteQuality
SIO_000300: 6.44e0

DP
type: SiteQuality
SIO_000300: 4.57025e5

VQSLOD
type: SiteQuality
SIO_000300: -1.968e0

GenotypeQuality
all individuals: 1906
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 63
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.219679064560268e-5
allele num: 16078
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3366
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2206
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.968e0

DP
type: SiteQuality
SIO_000300: 4.57025e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.66e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
SIO_000300: 6.44e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.034e0

FS
type: SiteQuality
SIO_000300: 2.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.8e-1

GenotypeQuality
all individuals: 5
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1208
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 226
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1828
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2952
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 2.204261572373255e-4
allele num: 13610
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.78e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.61e-2

QD
type: SiteQuality
SIO_000300: 1.307e1

DP
type: SiteQuality
SIO_000300: 4.32588e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.48e-1

GenotypeQuality
all individuals: 6
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1065
bin: 6.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1616
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1034
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.642544924720738e-4
allele num: 8236
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2688
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 516
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12358
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.21921e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.166e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.87e-2

QD
type: SiteQuality
SIO_000300: 4.76e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.67e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeQuality
all individuals: 70
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1946
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21647
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6569
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 740
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2144
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1360
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.965107057890563e-4
allele num: 7566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 468
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.39e0

QD
type: SiteQuality
SIO_000300: 1.179e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.05e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.017e0

DP
type: SiteQuality
SIO_000300: 4.2067e5

GenotypeQuality
all individuals: 26761
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 505
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 448
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1926
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1980
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.965243296921549e-5
allele num: 20140
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 7.8125e-4
allele num: 1280
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7552
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3902
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.214e0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 7.35e0

DP
type: SiteQuality
SIO_000300: 5.69889e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.99e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 4123
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4362
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3083
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2965
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1865
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4149
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 7.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3924
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2002
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.919323101141283e-5
allele num: 20328
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1306
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7594
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.444e-1

QD
type: SiteQuality
SIO_000300: 9.210000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.04e-1

DP
type: SiteQuality
SIO_000300: 5.79343e5

GenotypeQuality
all individuals: 226
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7979
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4062
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1786
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4810
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3968
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2058
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1954
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1340
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7696
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20684
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.22e-1

DP
type: SiteQuality
SIO_000300: 5.90929e5

QD
type: SiteQuality
SIO_000300: 1.815e1

GenotypeQuality
all individuals: 7300
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1519
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5784
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3898
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 334
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2224
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2354
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.392901071867862e-5
allele num: 22764
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8324
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4296
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.53e-2

FS
type: SiteQuality
SIO_000300: 3.746e0

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.866e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 3.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

QD
type: SiteQuality
SIO_000300: 8.0e0

DP
type: SiteQuality
SIO_000300: 6.44031e5

GenotypeQuality
all individuals: 312
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 115
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7378
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2416
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2282
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23152
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 5.917159763313609e-3
allele num: 338
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8378
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.42e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.412e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.78e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

FS
type: SiteQuality
SIO_000300: 2.199e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

QD
type: SiteQuality
SIO_000300: 2.464e1

DP
type: SiteQuality
SIO_000300: 6.50862e5

GenotypeQuality
all individuals: 104
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30737
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 970
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7677
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.260032376246059e-5
allele num: 23474
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1674
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2330
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.129e0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 3.432e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.261e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.46e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.457e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.58661e5

QD
type: SiteQuality
SIO_000300: 6.13e0

GenotypeQuality
all individuals: 995
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 223
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1461
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3412
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 503
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11902
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3102
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28182
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2206
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4990
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.02e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.61e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.307e0

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 7.4464e5

VQSLOD
type: SiteQuality
SIO_000300: -2.006e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 4.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

GenotypeQuality
all individuals: 328
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1459
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3157
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29470
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2315
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14605
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 7.25e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5342
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2484
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10032
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3264
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.91053e5

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

QD
type: SiteQuality
SIO_000300: 4.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.88e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.149e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-3

GenotypeQuality
all individuals: 17025
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 392
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2904
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1592
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1402
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.950897072710104e-5
allele num: 33888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2722
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5658
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4056
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.21e-1

DP
type: SiteQuality
SIO_000300: 8.33199e5

VQSLOD
type: SiteQuality
SIO_000300: -2.177e0

MQRankSum
type: SiteQuality
SIO_000300: -5.7e-1

QD
type: SiteQuality
SIO_000300: 2.86e0

GenotypeQuality
all individuals: 1368
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2578
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 129
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2741
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2932
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.600044800358403e-5
allele num: 35714
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 4.539264639128461e-4
allele num: 4406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10788
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5864
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.64894e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 7.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.05e-1

QD
type: SiteQuality
SIO_000300: 1.45e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.96e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 326
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1600
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33239
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2756
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 140
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6258
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8080
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8180
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.60225026607876e-5
allele num: 13154
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4620
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.93e-1

QD
type: SiteQuality
SIO_000300: 1.259e1

VQSLOD
type: SiteQuality
SIO_000300: 9.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.736e0

FS
type: SiteQuality
SIO_000300: 2.373e0

DP
type: SiteQuality
SIO_000300: 1.109752e6

GenotypeQuality
all individuals: 703
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 366
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41805
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3296
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 611
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 765
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9926
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5434
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7494
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.731361889262094e-5
allele num: 57758
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.455425017277125e-4
allele num: 14470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9056
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.221e0

MQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.078e0

DP
type: SiteQuality
SIO_000300: 1.234204e6

QD
type: SiteQuality
SIO_000300: 9.74e0

VQSLOD
type: SiteQuality
SIO_000300: -1.002e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 5.836e1

GenotypeQuality
all individuals: 385
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 591
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 759
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 587
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41925
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9122
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10040
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.719749604457591e-5
allele num: 58148
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.08e0

QD
type: SiteQuality
SIO_000300: 2.302e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.51e-1

FS
type: SiteQuality
SIO_000300: 3.637e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.26e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.087e0

DP
type: SiteQuality
SIO_000300: 1.244579e6

GenotypeQuality
all individuals: 401
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 771
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3472
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7808
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10420
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.677908654652841e-5
allele num: 59598
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14916
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.002e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.317e0

MQRankSum
type: SiteQuality
SIO_000300: 6.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.0e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.5e-1

DP
type: SiteQuality
SIO_000300: 1.270211e6

VQSLOD
type: SiteQuality
SIO_000300: 5.47e-1