10-97755900-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97755900
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97755900
    reference: chr 10
allele count: 3
allele frequency: 2.521008403361344e-4
allele num: 11900
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-45615C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+93123C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*609G>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+93123C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-74546C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.88G>A
  hgvsp: ENSP00000360241.2:p.Asp30Asn
  variant of: http://identifiers.org/hgnc/31666
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4900
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1138
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp30Asn
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/10-97755917-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97755917
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97755917
    reference: chr 10
allele count: 1
allele frequency: 8.238589553468446e-5
allele num: 12138
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+93106G>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.105C>A
  hgvsp: ENSP00000360241.2:p.Phe35Leu
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*626C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+93106G>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-45632G>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-74563G>T
  variant of: http://identifiers.org/hgnc/45203
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5150
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1206
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Phe35Leu
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

10-97755938-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97755938
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97755938
    reference: chr 10
allele count: 1
allele frequency: 8.175277959450622e-5
allele num: 12232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-74584G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-45653G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.126C>T
  hgvsp: ENST00000371198.2:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+93085G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*647C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+93085G>A
  variant of: http://identifiers.org/hgnc/45203
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1328
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5234
  bin: 6.25e1
  variant carriers: 0
hgvs: p.His42His
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-97755941-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97755941
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97755941
    reference: chr 10
allele count: 2
allele frequency: 1.634521085322001e-4
allele num: 12236
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+93082A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*650T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+93082A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-74587A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.129T>G
  hgvsp: ENST00000371198.2:c.129T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-45656A>C
  variant of: http://identifiers.org/hgnc/45203
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1249
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5236
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Thr43Thr
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

10-97755944-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97755944
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97755944
    reference: chr 10
allele count: 7
allele frequency: 5.719888870730511e-4
allele num: 12238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.132A>G
  hgvsp: ENST00000371198.2:c.132A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*653A>G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+93079T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-74590T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-45659T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+93079T>C
  variant of: http://identifiers.org/hgnc/45203
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5228
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1222
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 9.75e1
  variant carriers: 7
hgvs: p.Val44Val
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

10-97756038-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97756038
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97756038
    reference: chr 10
allele count: 2
allele frequency: 1.772735330615139e-4
allele num: 11282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+92985G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*718+29C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-74684G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+92985G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.197+29C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-45753G>A
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

10-97763859-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97763859
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97763859
    reference: chr 10
allele count: 2
allele frequency: 3.37029422668599e-5
allele num: 59342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85164T>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*719-50A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53574T>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.-76-50A>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.-76-50A>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.-76-50A>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.198-50A>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82505T>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85164T>A
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7652
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22281
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14781
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4795
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4862
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4827
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 8.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/10-97763873-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97763873
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97763873
    reference: chr 10
allele count: 155
allele frequency: 2.52731126691668e-3
allele num: 61330
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53588T>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.-76-36A>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82519T>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.-76-36A>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.198-36A>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85150T>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85150T>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.-76-36A>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*719-36A>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5733
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6431
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 14499
  bin: 1.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23322
  bin: 7.5e0
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3006
  bin: 1.75e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1775
  bin: 9.75e1
  variant carriers: 151
genotype quality: GenotypeQuality
  all individuals: 3795
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6644
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20289
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4619
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-97763888-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97763888
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97763888
    reference: chr 10
allele count: 74
allele frequency: 1.065668202764977e-3
allele num: 69440
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85135T>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.-76-21A>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.-76-21A>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53603T>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*719-21A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.-76-21A>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85135T>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82534T>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.198-21A>C
  variant of: http://identifiers.org/hgnc/31666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 1.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16658
  bin: 2.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2249
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8846
  bin: 1.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22915
  bin: 7.5e0
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22165
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 8.25e1
  variant carriers: 2
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: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

10-97763914-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97763914
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97763914
    reference: chr 10
allele count: 1
allele frequency: 9.240948490953111e-6
allele num: 108214
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.-71C>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.-71C>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82560G>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85109G>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*724C>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53629G>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.203C>G
  hgvsp: ENSP00000360241.2:p.Pro68Arg
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.-71C>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85109G>C
  variant of: http://identifiers.org/hgnc/45203
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5896
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6035
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro68Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

10-97763919-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97763919
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97763919
    reference: chr 10
allele count: 1
allele frequency: 8.993938085730218e-6
allele num: 111186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85104G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85104G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53634G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.208C>T
  hgvsp: ENSP00000360241.2:p.His70Tyr
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*729C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82565G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.-66C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.-66C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.-66C>T
  variant of: http://identifiers.org/hgnc/31666
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8590
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1563
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His70Tyr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

10-97763939-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97763939
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97763939
    reference: chr 10
allele count: 1
allele frequency: 8.513826454161559e-6
allele num: 117456
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.228C>T
  hgvsp: ENST00000371198.2:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.-46C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85084G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53654G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.-46C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.-46C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85084G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82585G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*749C>T
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 756
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1556
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser76Ser
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

10-97763940-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97763940
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97763940
    reference: chr 10
allele count: 1
allele frequency: 8.498053945646446e-6
allele num: 117674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.-45T>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*750T>A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85083A>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.229T>A
  hgvsp: ENSP00000360241.2:p.Leu77Ile
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.-45T>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85083A>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.-45T>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82586A>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53655A>T
  variant of: http://identifiers.org/hgnc/45203
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42020
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4183
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1740
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1888
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2301
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu77Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

10-97763943-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97763943
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97763943
    reference: chr 10
allele count: 1
allele frequency: 8.457088731774973e-6
allele num: 118244
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.-42T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.232T>C
  hgvsp: ENSP00000360241.2:p.Ser78Pro
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85080A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*753T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85080A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.-42T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.-42T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53658A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82589A>G
  variant of: http://identifiers.org/hgnc/45203
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42228
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1170
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1982
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6009
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser78Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

10-97763949-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97763949
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97763949
    reference: chr 10
allele count: 1
allele frequency: 8.404915194405689e-6
allele num: 118978
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53664T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.238A>G
  hgvsp: ENSP00000360241.2:p.Ile80Val
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*759A>G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.-36A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.-36A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85074T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.-36A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82595T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85074T>C
  variant of: http://identifiers.org/hgnc/45203
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6085
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile80Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

10-97763956-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97763956
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97763956
    reference: chr 10
allele count: 1
allele frequency: 8.367640660039494e-6
allele num: 119508
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.245A>T
  hgvsp: ENSP00000360241.2:p.Asp82Val
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85067T>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.-29A>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.-29A>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82602T>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85067T>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.-29A>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*766A>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53671T>A
  variant of: http://identifiers.org/hgnc/45203
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10238
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1966
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6152
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp82Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

10-97763972-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97763972
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97763972
    reference: chr 10
allele count: 1
allele frequency: 8.340005337603416e-6
allele num: 119904
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53687G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.-13C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.-13C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.261C>T
  hgvsp: ENST00000371198.2:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*782C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85051G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85051G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.-13C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82618G>A
  variant of: http://identifiers.org/hgnc/45203
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2011
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn87Asn
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD

10-97763974-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97763974
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97763974
    reference: chr 10
allele count: 7
allele frequency: 5.838782864006406e-5
allele num: 119888
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82620A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85049A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.-11T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.-11T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.263T>C
  hgvsp: ENSP00000360241.2:p.Ile88Thr
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.-11T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85049A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53689A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*784T>C
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4433
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10301
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1978
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1825
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43536
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile88Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-97763999-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97763999
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97763999
    reference: chr 10
allele count: 2
allele frequency: 1.676951972095519e-5
allele num: 119264
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82645T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.15A>G
  hgvsp: ENST00000424464.1:c.15A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85024T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85024T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.15A>G
  hgvsp: ENST00000410012.2:c.15A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.15A>G
  hgvsp: ENST00000344386.3:c.15A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53714T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*809A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.288A>G
  hgvsp: ENST00000371198.2:c.288A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9696
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys5Lys
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

10-97764001-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97764001
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97764001
    reference: chr 10
allele count: 1
allele frequency: 8.390106386548982e-6
allele num: 119188
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85022T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.17A>G
  hgvsp: ENSP00000391834.1:p.His6Arg
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.290A>G
  hgvsp: ENSP00000360241.2:p.His97Arg
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53716T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.17A>G
  hgvsp: ENSP00000386988.2:p.His6Arg
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*811A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.17A>G
  hgvsp: ENSP00000343747.3:p.His6Arg
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85022T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82647T>C
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9665
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5944
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2016
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
hgvs: p.His6Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum

10-97764013-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97764013
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97764013
    reference: chr 10
allele count: 4
allele frequency: 3.3716010047371e-5
allele num: 118638
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.294+8A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85010T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53728T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*815+8A>G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.21+8A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.21+8A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82659T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.21+8A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85010T>C
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1636
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 7.25e1
  variant carriers: 0
hgvs: c.21+8A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

10-97764014-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97764014
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97764013
    reference: chr 10
allele count: 7
allele frequency: 5.906475184366404e-5
allele num: 118514
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.21+11delA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53730delT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85008delT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85008delT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.294+11delA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.21+11delA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*815+11delA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82661delT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.21+11delA
  variant of: http://identifiers.org/hgnc/31666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8872
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5715
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2078
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: GA
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

10-97764014-GAAT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97764014
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97764011
    reference: chr 10
allele count: 57
allele frequency: 4.809558364412643e-4
allele num: 118514
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.21+13_21+15delAAT
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.21+13_21+15delAAT
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53732_260-53730delATT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82663_274-82661delATT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85006_275+85008delATT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85006_216+85008delATT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*815+13_*815+15delAAT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.294+13_294+15delAAT
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.21+13_21+15delAAT
  variant of: http://identifiers.org/hgnc/31666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3919
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8872
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 42026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 9.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5715
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2352
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: GAAT
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

10-97764022-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97764022
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97764022
    reference: chr 10
allele count: 10
allele frequency: 8.460666362082677e-5
allele num: 118194
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.21+17A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.21+17A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.21+17A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53737T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.294+17A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+85001T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82668T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+85001T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*815+17A>G
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8306
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3787
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 1803
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2081
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

10-97764026-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97764026
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97764026
    reference: chr 10
allele count: 1
allele frequency: 8.487379267029927e-6
allele num: 117822
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+84997A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.21+21T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*815+21T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.21+21T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82672A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.294+21T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.21+21T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+84997A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53741A>G
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 810
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 769
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: T
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

10-97764027-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97764027
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97764027
    reference: chr 10
allele count: 1
allele frequency: 8.484066922319883e-6
allele num: 117868
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.294+22A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.21+22A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*815+22A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.21+22A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53742T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+84996T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82673T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.21+22A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+84996T>C
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3738
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8063
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1871
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1802
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-97764029-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97764029
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97764029
    reference: chr 10
allele count: 1
allele frequency: 8.499209573509664e-6
allele num: 117658
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.21+24C>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+84994G>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82675G>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.21+24C>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53744G>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*815+24C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.294+24C>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+84994G>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.21+24C>A
  variant of: http://identifiers.org/hgnc/31666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2084
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40227
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1801
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/10-97764031-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97764031
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97764031
    reference: chr 10
allele count: 1
allele frequency: 8.501666326600013e-6
allele num: 117624
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+84992T>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82677T>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.21+26A>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.21+26A>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53746T>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.21+26A>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.294+26A>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+84992T>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*815+26A>C
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3711
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40053
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

10-97764035-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97764035
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97764035
    reference: chr 10
allele count: 1
allele frequency: 8.519484060045324e-6
allele num: 117378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82681G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.21+30C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.21+30C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*815+30C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+84988G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.21+30C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.294+30C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+84988G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53750G>A
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7840
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1801
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

10-97764045-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97764045
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97764045
    reference: chr 10
allele count: 1
allele frequency: 8.54978540038645e-6
allele num: 116962
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.21+40T>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+84978A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*815+40T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82691A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.294+40T>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.21+40T>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.21+40T>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+84978A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53760A>C
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5502
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2236
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1800
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 740
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP

10-97764046-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97764046
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97764046
    reference: chr 10
allele count: 8
allele frequency: 6.851426809633107e-5
allele num: 116764
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53761G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.21+41C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.21+41C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*815+41C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.294+41C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82692G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+84977G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+84977G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.21+41C>T
  variant of: http://identifiers.org/hgnc/31666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7705
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41013
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1863
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/10-97764053-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97764053
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97764052
    reference: chr 10
allele count: 2
allele frequency: 1.718272105570638e-5
allele num: 116396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+84969delT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+84969delT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-53769delT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*815+51delA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.21+51delA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.294+51delA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.274-82700delT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.21+51delA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.21+51delA
  variant of: http://identifiers.org/hgnc/31666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7716
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2346
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38860
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: CA
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

10-97769538-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769538
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769538
    reference: chr 10
allele count: 1
allele frequency: 1.205836247437598e-5
allele num: 82930
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79485G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.295-44C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.22-44C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59253G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79485G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.22-44C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.22-44C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79485G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*816-44C>T
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14448
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9331
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1750
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2124
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

10-97769545-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769545
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769545
    reference: chr 10
allele count: 2
allele frequency: 2.380442286176772e-5
allele num: 84018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59260A>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.22-37T>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.295-37T>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79478A>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79478A>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*816-37T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.22-37T>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79478A>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.22-37T>A
  variant of: http://identifiers.org/hgnc/31666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 747
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11911
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1617
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5899
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3342
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4759
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1804
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 971
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum

10-97769547-TTAAG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769547
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769543
    reference: chr 10
allele count: 2
allele frequency: 2.376256445595609e-5
allele num: 84166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59266_260-59263delCTTA
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79472_273+79475delCTTA
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.22-27_22-24delGTAA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.22-27_22-24delGTAA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.295-27_295-24delGTAA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*816-27_*816-24delGTAA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.22-27_22-24delGTAA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79472_216+79475delCTTA
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79472_275+79475delCTTA
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12449
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3725
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5570
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2469
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 848
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3286
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: TTAAG
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

10-97769551-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769551
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769551
    reference: chr 10
allele count: 1
allele frequency: 1.176027848339449e-5
allele num: 85032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79472C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59266C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*816-31G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.22-31G>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.22-31G>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79472C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.22-31G>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79472C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.295-31G>A
  variant of: http://identifiers.org/hgnc/31666
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12748
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4144
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3840
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4120
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

10-97769562-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769562
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769562
    reference: chr 10
allele count: 1
allele frequency: 1.05909764880322e-5
allele num: 94420
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59277T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.22-20A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79461T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79461T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*816-20A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.22-20A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.295-20A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79461T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.22-20A>G
  variant of: http://identifiers.org/hgnc/31666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11685
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2205
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5731
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30662
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1702
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1488
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11624
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS

10-97769566-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769566
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769566
    reference: chr 10
allele count: 12
allele frequency: 1.210018956963659e-4
allele num: 99172
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79457A>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79457A>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.22-16T>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79457A>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.22-16T>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.295-16T>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*816-16T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.22-16T>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59281A>T
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34015
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9907
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9902
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1502
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

10-97769567-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769567
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769567
    reference: chr 10
allele count: 1
allele frequency: 9.952031209569873e-6
allele num: 100482
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79456A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.22-15T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79456A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59282A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.295-15T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.22-15T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.22-15T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79456A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*816-15T>C
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

10-97769589-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769589
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769589
    reference: chr 10
allele count: 3
allele frequency: 2.507899884636605e-5
allele num: 119622
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79434C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79434C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.29G>A
  hgvsp: ENSP00000391834.1:p.Cys10Tyr
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.29G>A
  hgvsp: ENSP00000343747.3:p.Cys10Tyr
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.29G>A
  hgvsp: ENSP00000386988.2:p.Cys10Tyr
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.302G>A
  hgvsp: ENSP00000360241.2:p.Cys101Tyr
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59304C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79434C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*823G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2816
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44445
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8204
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Cys10Tyr
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

10-97769595-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769595
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769595
    reference: chr 10
allele count: 1
allele frequency: 8.334722453742291e-6
allele num: 119980
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79428T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79428T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.35A>G
  hgvsp: ENSP00000391834.1:p.Lys12Arg
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59310T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.308A>G
  hgvsp: ENSP00000360241.2:p.Lys103Arg
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.35A>G
  hgvsp: ENSP00000386988.2:p.Lys12Arg
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79428T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.35A>G
  hgvsp: ENSP00000343747.3:p.Lys12Arg
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*829A>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3882
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys12Arg
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

10-97769604-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769604
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769604
    reference: chr 10
allele count: 1
allele frequency: 8.319605983460623e-6
allele num: 120198
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79419C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79419C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.317G>A
  hgvsp: ENSP00000360241.2:p.Ser106Asn
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.44G>A
  hgvsp: ENSP00000391834.1:p.Ser15Asn
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79419C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.44G>A
  hgvsp: ENSP00000343747.3:p.Ser15Asn
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*838G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.44G>A
  hgvsp: ENSP00000386988.2:p.Ser15Asn
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59319C>T
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser15Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

10-97769607-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769607
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769607
    reference: chr 10
allele count: 3
allele frequency: 2.49513448774889e-5
allele num: 120234
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79416C>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79416C>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.47G>T
  hgvsp: ENSP00000386988.2:p.Gly16Val
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.47G>T
  hgvsp: ENSP00000343747.3:p.Gly16Val
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.47G>T
  hgvsp: ENSP00000391834.1:p.Gly16Val
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59322C>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*841G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.320G>T
  hgvsp: ENSP00000360241.2:p.Gly107Val
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79416C>A
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8492
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1028
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly16Val
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

10-97769613-CATAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769613
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769609
    reference: chr 10
allele count: 1
allele frequency: 8.31255195344971e-6
allele num: 120300
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79406_216+79409delATAT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.57_60delTATA
  hgvsp: ENSP00000391834.1:p.Tyr19Ter
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.330_333delTATA
  hgvsp: ENSP00000360241.2:p.Tyr110Ter
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79406_273+79409delATAT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.57_60delTATA
  hgvsp: ENSP00000386988.2:p.Tyr19Ter
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.57_60delTATA
  hgvsp: ENSP00000343747.3:p.Tyr19Ter
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79406_275+79409delATAT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*851_*854delTATA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59332_260-59329delATAT
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8523
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3880
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Tyr19Ter
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: CATAT
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

10-97769615-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769615
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769615
    reference: chr 10
allele count: 2
allele frequency: 1.662289304830613e-5
allele num: 120316
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.55T>C
  hgvsp: ENSP00000343747.3:p.Tyr19His
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*849T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.328T>C
  hgvsp: ENSP00000360241.2:p.Tyr110His
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79408A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.55T>C
  hgvsp: ENSP00000391834.1:p.Tyr19His
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79408A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.55T>C
  hgvsp: ENSP00000386988.2:p.Tyr19His
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59330A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79408A>G
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3882
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4875
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Tyr19His
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

10-97769618-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769618
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769618
    reference: chr 10
allele count: 2
allele frequency: 1.6619025460347e-5
allele num: 120344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79405T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.58A>G
  hgvsp: ENSP00000343747.3:p.Ile20Val
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79405T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.331A>G
  hgvsp: ENSP00000360241.2:p.Ile111Val
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.58A>G
  hgvsp: ENSP00000386988.2:p.Ile20Val
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59333T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79405T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*852A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.58A>G
  hgvsp: ENSP00000391834.1:p.Ile20Val
  variant of: http://identifiers.org/hgnc/31666
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8543
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1285
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4873
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1614
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile20Val
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

10-97769639-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769639
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769639
    reference: chr 10
allele count: 1
allele frequency: 8.306337735692333e-6
allele num: 120390
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79384A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79384A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.79T>G
  hgvsp: ENSP00000391834.1:p.Cys27Gly
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59354A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.79T>G
  hgvsp: ENSP00000343747.3:p.Cys27Gly
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*873T>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.352T>G
  hgvsp: ENSP00000360241.2:p.Cys118Gly
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.79T>G
  hgvsp: ENSP00000386988.2:p.Cys27Gly
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79384A>C
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Cys27Gly
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ

10-97769640-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769640
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769640
    reference: chr 10
allele count: 2
allele frequency: 1.661157162079104e-5
allele num: 120398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79383C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*874G>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59355C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.80G>A
  hgvsp: ENSP00000386988.2:p.Cys27Tyr
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.80G>A
  hgvsp: ENSP00000343747.3:p.Cys27Tyr
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.80G>A
  hgvsp: ENSP00000391834.1:p.Cys27Tyr
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.353G>A
  hgvsp: ENSP00000360241.2:p.Cys118Tyr
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79383C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79383C>T
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44444
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3890
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 46441
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys27Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

10-97769657-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769657
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769657
    reference: chr 10
allele count: 1
allele frequency: 8.314072398942449e-6
allele num: 120278
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79366A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.97T>G
  hgvsp: ENSP00000386988.2:p.Ser33Ala
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59372A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79366A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.97T>G
  hgvsp: ENSP00000343747.3:p.Ser33Ala
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.97T>G
  hgvsp: ENSP00000391834.1:p.Ser33Ala
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.370T>G
  hgvsp: ENSP00000360241.2:p.Ser124Ala
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79366A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*891T>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44217
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8614
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 407
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1273
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser33Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

10-97769667-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769667
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769667
    reference: chr 10
allele count: 1
allele frequency: 8.321129010784183e-6
allele num: 120176
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59382A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79356A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.107T>C
  hgvsp: ENSP00000391834.1:p.Leu36Pro
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.107T>C
  hgvsp: ENSP00000386988.2:p.Leu36Pro
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*901T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79356A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.380T>C
  hgvsp: ENSP00000360241.2:p.Leu127Pro
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.107T>C
  hgvsp: ENSP00000343747.3:p.Leu36Pro
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79356A>G
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44074
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1608
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1269
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu36Pro
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

10-97769668-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769668
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769668
    reference: chr 10
allele count: 4
allele frequency: 3.328562393902073e-5
allele num: 120172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79355C>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.108G>T
  hgvsp: ENST00000344386.3:c.108G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.108G>T
  hgvsp: ENST00000424464.1:c.108G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79355C>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.381G>T
  hgvsp: ENST00000371198.2:c.381G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59383C>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.108G>T
  hgvsp: ENST00000410012.2:c.108G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*902G>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79355C>A
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4820
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1605
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu36Leu
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP

10-97769671-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769671
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769671
    reference: chr 10
allele count: 1
allele frequency: 8.322652595835345e-6
allele num: 120154
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59386T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*905A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.111A>G
  hgvsp: ENST00000344386.3:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79352T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.111A>G
  hgvsp: ENST00000410012.2:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79352T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.384A>G
  hgvsp: ENST00000371198.2:c.384A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.111A>G
  hgvsp: ENST00000424464.1:c.111A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79352T>C
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln37Gln
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

10-97769687-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769687
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769686
    reference: chr 10
allele count: 20
allele frequency: 1.66908684258842e-4
allele num: 119826
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+11delA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.120+11delA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.120+11delA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.120+11delA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59403delT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79335delT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+11delA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79335delT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79335delT
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2839
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43239
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1595
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45199
  bin: 6.25e1
  variant carriers: 0
hgvs: c.120+11delA
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: GA
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

10-97769688-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769688
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769688
    reference: chr 10
allele count: 1
allele frequency: 8.349336227769892e-6
allele num: 119770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.120+8A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79335T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79335T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.120+8A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+8A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59403T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.120+8A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+8A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79335T>C
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43161
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4745
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1026
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
hgvs: c.120+8A>G
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

10-97769696-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769696
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769696
    reference: chr 10
allele count: 37
allele frequency: 3.095768001472582e-4
allele num: 119518
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+16T>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79327A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+16T>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.120+16T>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79327A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79327A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.120+16T>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59411A>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.120+16T>G
  variant of: http://identifiers.org/hgnc/31666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2801
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8333
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41761
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43344
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4653
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ

10-97769712-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769712
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769712
    reference: chr 10
allele count: 2
allele frequency: 1.6787255115916e-5
allele num: 119138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79311C>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+32G>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59427C>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.120+32G>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.120+32G>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+32G>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79311C>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.120+32G>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79311C>G
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8086
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37813
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1888
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2227
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1425
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39075
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1573
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

10-97769718-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769718
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769718
    reference: chr 10
allele count: 4
allele frequency: 3.364228161953944e-5
allele num: 118898
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+38A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+38A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79305T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.120+38A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.120+38A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59433T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79305T>C
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.120+38A>G
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79305T>C
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6250
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7737
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2421
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/10-97769719-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769719
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769719
    reference: chr 10
allele count: 1
allele frequency: 8.415100055539661e-6
allele num: 118834
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.120+39C>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79304G>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+39C>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.120+39C>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79304G>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+39C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59434G>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.120+39C>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79304G>T
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7724
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6948
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1013
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1566
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1466
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1240
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

10-97769728-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769728
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769728
    reference: chr 10
allele count: 1
allele frequency: 8.4774499830451e-6
allele num: 117960
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+48C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59443G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79295G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.120+48C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79295G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.120+48C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79295G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+48C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.120+48C>T
  variant of: http://identifiers.org/hgnc/31666
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8572
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31551
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1582
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3883
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

10-97769728-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97769728
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97769726
    reference: chr 10
allele count: 1
allele frequency: 8.4774499830451e-6
allele num: 117960
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+50_393+51delTA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.120+50_120+51delTA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.120+50_120+51delTA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.120+50_120+51delTA
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+50_*914+51delTA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+79293_216+79294delAT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+79293_273+79294delAT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+79293_275+79294delAT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-59445_260-59444delAT
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8572
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1587
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3901
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3720
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3262
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: CAT
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ

10-97772007-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97772007
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97772007
    reference: chr 10
allele count: 3
allele frequency: 1.94300518134715e-4
allele num: 15440
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+77016A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.186T>C
  hgvsp: ENST00000424464.1:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+77016A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+2327T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+77016A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-61722A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.121-282T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.121-282T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+2327T>C
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4716
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3437
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3151
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1127
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr62Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: T
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

10-97772084-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97772084
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97772084
    reference: chr 10
allele count: 1
allele frequency: 7.992327365728901e-5
allele num: 12512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+76939G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.121-205C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.121-205C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.263C>T
  hgvsp: ENSP00000391834.1:p.Pro88Leu
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+2404C>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+76939G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+2404C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+76939G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-61799G>A
  variant of: http://identifiers.org/hgnc/45203
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11198
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro88Leu
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

10-97772092-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97772092
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97772092
    reference: chr 10
allele count: 29
allele frequency: 2.396298132540076e-3
allele num: 12102
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+76931A>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.121-197T>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.271T>A
  hgvsp: ENSP00000391834.1:p.Ser91Thr
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.121-197T>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+76931A>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+2412T>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-61807A>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+76931A>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+2412T>A
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13822
  bin: 2.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2447
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser91Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

10-97772093-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97772093
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97772091
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 11914
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+76928_216+76929delAT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+76928_275+76929delAT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+2416_*914+2417delAT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-61810_260-61809delAT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+2416_393+2417delAT
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.121-193_121-192delAT
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+76928_273+76929delAT
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.275_276delAT
  hgvsp: ENSP00000391834.1:p.Tyr92CysfsTer4
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.121-193_121-192delAT
  variant of: http://identifiers.org/hgnc/31666
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14019
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1296
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Tyr92CysfsTer4
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: CAT
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum

10-97772102-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97772102
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97772102
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 11468
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+76921G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+2422C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-61817G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.281C>T
  hgvsp: ENSP00000391834.1:p.Thr94Ile
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+76921G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+76921G>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.121-187C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.121-187C>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+2422C>T
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16287
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4980
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr94Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS

10-97772124-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97772124
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97772124
    reference: chr 10
allele count: 1
allele frequency: 9.554748710108924e-5
allele num: 10466
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-61839C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+2444G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+2444G>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.121-165G>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.121-165G>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.303G>A
  hgvsp: ENST00000424464.1:c.303G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+76899C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+76899C>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+76899C>T
  variant of: http://identifiers.org/hgnc/45203
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4745
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23355
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5154
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21395
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2061
  bin: 2.5e0
  variant carriers: 0
hgvs: c.303G>A
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/10-97772145-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97772145
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97772145
    reference: chr 10
allele count: 1
allele frequency: 1.019367991845056e-4
allele num: 9810
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+2465C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+76878G>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+76878G>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.121-144C>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+2465C>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+76878G>T
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.303+21C>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.121-144C>A
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-61860G>T
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31046
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1311
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5596
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

10-97772147-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97772147
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97772147
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 9824
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.121-142T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.121-142T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+2467T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+2467T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-61862A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+76876A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.303+23T>C
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+76876A>G
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+76876A>G
  variant of: http://identifiers.org/hgnc/45203
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1780
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6726
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31614
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29184
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-97772152-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97772152
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97772152
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 9848
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.121-137A>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+2472A>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.303+28A>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+2472A>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+76871T>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-61867T>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+76871T>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+76871T>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.121-137A>T
  variant of: http://identifiers.org/hgnc/31666
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7648
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6326
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2400
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30835
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

10-97772163-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 97772163
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 97772163
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 10600
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000454638
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000454638.1:n.273+76860T>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000386988
  ensembl transcript: ENST00000410012
  gene symbol: CC2D2B
  hgvsc: ENST00000410012.2:c.121-126A>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000343747
  ensembl transcript: ENST00000344386
  gene symbol: CC2D2B
  hgvsc: ENST00000344386.3:c.121-126A>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000360241
  ensembl transcript: ENST00000371198
  gene symbol: CC2D2B
  hgvsc: ENST00000371198.2:c.393+2483A>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000188649
  ensembl protein: ENSP00000391834
  ensembl transcript: ENST00000424464
  gene symbol: CC2D2B
  hgvsc: ENST00000424464.1:c.303+39A>T
  variant of: http://identifiers.org/hgnc/31666
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000416301
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000416301.1:n.275+76860T>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000451364
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000451364.1:n.216+76860T>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000226688
  ensembl transcript: ENST00000452728
  gene symbol: ENTPD1-AS1
  hgvsc: ENST00000452728.1:n.260-61878T>A
  variant of: http://identifiers.org/hgnc/45203
annotation: Annotation
  canonical: true
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000269920
  ensembl protein: ENSP00000473319
  ensembl transcript: ENST00000475252
  gene symbol: RP11-690P14.4
  hgvsc: ENST00000475252.2:c.*914+2483A>T
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11464
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34798
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1680
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9573
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.798561151079137e-3
allele num: 556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.763688760806917e-4
allele num: 3470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7358
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.94e-2

FS
type: SiteQuality
SIO_000300: 7.275e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.252e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.54e-1

QD
type: SiteQuality
SIO_000300: 1.197e1

DP
type: SiteQuality
SIO_000300: 1.45975e5

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

GenotypeQuality
all individuals: 26
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 127
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 95
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 93
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.328727079457879e-4
allele num: 7526
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3534
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.247999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.22e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

VQSLOD
type: SiteQuality
SIO_000300: -1.99e0

DP
type: SiteQuality
SIO_000300: 1.50131e5

MQRankSum
type: SiteQuality
SIO_000300: -1.618e0

QD
type: SiteQuality
SIO_000300: 8.49e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.269e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e0

GenotypeQuality
all individuals: 35
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1210
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 7.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.319609395618897e-4
allele num: 7578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.524e0

FS
type: SiteQuality
SIO_000300: 2.706e0

DP
type: SiteQuality
SIO_000300: 1.51053e5

QD
type: SiteQuality
SIO_000300: 5.88e0

VQSLOD
type: SiteQuality
SIO_000300: -1.871e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.24e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.183e0

GenotypeQuality
all individuals: 61
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 93
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.638522427440633e-4
allele num: 7580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3578
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.66e-1

DP
type: SiteQuality
SIO_000300: 1.51097e5

FS
type: SiteQuality
SIO_000300: 8.81e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
type: SiteQuality
SIO_000300: 9.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.398e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.16e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.57e-1

QD
type: SiteQuality
SIO_000300: 8.390000000000001e0

GenotypeQuality
all individuals: 61
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 72
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7580
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.792114695340502e-3
allele num: 558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.675977653631285e-3
allele num: 3580
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.163e1

MQ
type: SiteQuality
SIO_000300: 5.951e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e-1

FS
type: SiteQuality
SIO_000300: 1.745e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.51234e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.15e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.87e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.24e-1

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 763
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1343
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2055
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6884
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.636363636363636e-3
allele num: 550
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3346
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.3e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.912e0

MQRankSum
type: SiteQuality
SIO_000300: 2.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.82e-2

FS
type: SiteQuality
SIO_000300: 9.330000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.16853e5

VQSLOD
type: SiteQuality
SIO_000300: -3.783e-1

QD
type: SiteQuality
SIO_000300: 1.209e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.92e-1

GenotypeQuality
all individuals: 12087
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6840
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1501
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7907
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3648
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1341
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1973
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4172
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28768
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 5.037783375314861e-4
allele num: 3970
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 542
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5194
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4838
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11916
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.106e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.19e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.13e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.82e-1

FS
type: SiteQuality
SIO_000300: 5.07e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.04e-1

QD
type: SiteQuality
SIO_000300: 1.018e1

DP
type: SiteQuality
SIO_000300: 7.6937e5

GenotypeQuality
all individuals: 1525
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 191
bin: 9.25e1
variant carriers: 10

GenotypeQuality
all individuals: 1893
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1095
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1076
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 488
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4829
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 8322
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 8.75e1
variant carriers: 11

GenotypeQuality
all individuals: 484
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 315
bin: 8.25e1
variant carriers: 6

European (Non-Finnish)
type: Population
allele count: 110
allele frequency: 3.6855860081753e-3
allele num: 29846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4190
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 6.012024048096192e-4
allele num: 4990
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 4.757373929590866e-4
allele num: 4204
num of homozygotes: 0

South Asian
type: Population
allele count: 25
allele frequency: 2.070221927790659e-3
allele num: 12076
num of homozygotes: 0

Latino
type: Population
allele count: 15
allele frequency: 2.75027502750275e-3
allele num: 5454
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.01e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

DP
type: SiteQuality
SIO_000300: 8.17496e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
SIO_000300: 1.475e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

GenotypeQuality
all individuals: 1782
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2275
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2174
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4021
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3532
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 17914
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1723
bin: 9.75e1
variant carriers: 73

GenotypeQuality
all individuals: 632
bin: 7.25e1
variant carriers: 2

Latino
type: Population
allele count: 3
allele frequency: 4.448398576512455e-4
allele num: 6744
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4928
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12638
num of homozygotes: 0

African
type: Population
allele count: 70
allele frequency: 1.237623762376238e-2
allele num: 5656
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4648
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.923121894182987e-5
allele num: 34210
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

FS
type: SiteQuality
SIO_000300: 3.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.518e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.4e-3

DP
type: SiteQuality
SIO_000300: 9.62234e5

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

GenotypeQuality
all individuals: 264
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.709810894915022e-5
allele num: 58486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7746
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10784
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15576
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6294
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.26e-1

FS
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SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 5.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

QD
type: SiteQuality
SIO_000300: 1.581e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.851e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10992
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.337135614702154e-5
allele num: 15780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8742
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7916
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 5.32e0

FS
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MQRankSum
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BaseQRankSum
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DP
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SIO_000300: 1.387149e6

InbreedingCoeff
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SIO_000300: 3.5e-3

VQSLOD
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ClippingRankSum
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SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.79e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9378
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545738399233314e-5
allele num: 64694
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.523e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 2.348e0

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.939e1

BaseQRankSum
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SIO_000300: -1.16e0

MQRankSum
type: SiteQuality
SIO_000300: -4.91e-1

DP
type: SiteQuality
SIO_000300: 1.454671e6

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.09e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9388
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.169792694965449e-5
allele num: 16208
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11412
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.279999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: -1.804e0

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.95e1

VQSLOD
type: SiteQuality
SIO_000300: -1.198e0

FS
type: SiteQuality
SIO_000300: 2.791e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.48e-1

DP
type: SiteQuality
SIO_000300: 1.45687e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.55e-1

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16252
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.741258741258741e-5
allele num: 11440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65210
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9458
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.21e-1

QD
type: SiteQuality
SIO_000300: 1.454e1

VQSLOD
type: SiteQuality
SIO_000300: 2.52e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.91e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 1.462742e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.562e0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11486
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.174812030075188e-4
allele num: 8512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65678
num of homozygotes: 0

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

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

South Asian
type: Population
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 4.571e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.515059693351918e-5
allele num: 66004
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
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QD
type: SiteQuality
SIO_000300: 1.072e1

MQRankSum
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SIO_000300: 1.39e-1

VQSLOD
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508113651444773e-5
allele num: 66308
num of homozygotes: 0

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

East Asian
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South Asian
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
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MQ
type: SiteQuality
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.508022680661117e-5
allele num: 66312
num of homozygotes: 0

South Asian
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allele frequency: 3.698680803846628e-4
allele num: 16222
num of homozygotes: 0

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

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

Other
type: Population
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allele frequency: 0.0e0
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DP
type: SiteQuality
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MQRankSum
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MQ
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InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.29e0

QD
type: SiteQuality
SIO_000300: 1.481e1

FS
type: SiteQuality
SIO_000300: 5.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2016
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42628
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1817
bin: 8.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.018594542381067e-5
allele num: 66256
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.74e0

VQSLOD
type: SiteQuality
SIO_000300: -4.072e-1

QD
type: SiteQuality
SIO_000300: 9.289999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.25e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

DP
type: SiteQuality
SIO_000300: 1.464842e6

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66230
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 9.59e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.32e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.03e-1

DP
type: SiteQuality
SIO_000300: 1.463215e6

MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.67e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.652e0

FS
type: SiteQuality
SIO_000300: 1.747e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66094
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.647920055775041e-4
allele num: 8606
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: 11538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15198
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 9.91e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 4.1e0

QD
type: SiteQuality
SIO_000300: 1.313e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-1

DP
type: SiteQuality
SIO_000300: 1.44479e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.85e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.059482367186318e-4
allele num: 66070
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15104
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.447712e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.877e1

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.26e0

QD
type: SiteQuality
SIO_000300: 1.754e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.5e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 57

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.1441647597254e-3
allele num: 874
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15104
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.058681185722928e-3
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 49
allele frequency: 7.416376570304223e-4
allele num: 66070
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.26e0

MQ
type: SiteQuality
SIO_000300: 5.877e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.45e-1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.447712e6

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.5e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14852
num of homozygotes: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.16333178222429e-3
allele num: 8596
num of homozygotes: 0

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

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

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

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

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.14e-1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 4.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14584
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9700
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.516852228255923e-5
allele num: 65926
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.357e1

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -3.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516714190377965e-5
allele num: 65932
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9700
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14618
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e0

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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QD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.266e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 80
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.517727051966974e-5
allele num: 65888
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South Asian
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East Asian
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InbreedingCoeff
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ClippingRankSum
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FS
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VQSLOD
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MQRankSum
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QD
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BaseQRankSum
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ReadPosRankSum
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 1.031353135313531e-4
allele num: 9696
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65892
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Latino
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allele num: 11540
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
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Other
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allele frequency: 0.0e0
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East Asian
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FS
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DP
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MQ
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MQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 1.0315659170621e-4
allele num: 9694
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65824
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East Asian
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allele frequency: 0.0e0
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Latino
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VQSLOD
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DP
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FS
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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ReadPosRankSum
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

African
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allele frequency: 1.032204789430223e-4
allele num: 9688
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 65748
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Other
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allele frequency: 0.0e0
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Latino
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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FS
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13792
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European (Non-Finnish)
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allele count: 4
allele frequency: 6.089021494245874e-5
allele num: 65692
num of homozygotes: 0

Latino
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allele frequency: 3.46860908775581e-4
allele num: 11532
num of homozygotes: 0

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

European (Finnish)
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East Asian
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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
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allele num: 11530
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ClippingRankSum
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FS
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MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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BaseQRankSum
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MQ
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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Other
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European (Non-Finnish)
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African
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East Asian
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South Asian
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InbreedingCoeff
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MQ
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VQSLOD
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ClippingRankSum
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FS
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MQRankSum
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BaseQRankSum
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DP
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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European (Finnish)
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Latino
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Other
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African
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European (Non-Finnish)
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VQSLOD
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ReadPosRankSum
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MQ
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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QD
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FS
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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African
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Other
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European (Non-Finnish)
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allele num: 46720
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Latino
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South Asian
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MQRankSum
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ClippingRankSum
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DP
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MQ
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InbreedingCoeff
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ReadPosRankSum
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QD
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FS
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7026
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4172
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47220
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.750437521876094e-5
allele num: 11428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4692
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.148331e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.117e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e-1

QD
type: SiteQuality
SIO_000300: 2.71e0

VQSLOD
type: SiteQuality
SIO_000300: -2.794e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10464
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7538
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12460
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.914095398514662e-5
allele num: 52244
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5492
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 758
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.62e0

VQSLOD
type: SiteQuality
SIO_000300: 2.88e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.12e-1

DP
type: SiteQuality
SIO_000300: 1.316459e6

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.013e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.59e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 12

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13034
num of homozygotes: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.6e-3
allele num: 6250
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5850
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.262626262626263e-3
allele num: 792
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.828287260494369e-5
allele num: 54696
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10670
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.29e-2

QD
type: SiteQuality
SIO_000300: 1.817e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.35e0

DP
type: SiteQuality
SIO_000300: 1.368808e6

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.12e0

FS
type: SiteQuality
SIO_000300: 1.093e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8000
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5960
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55344
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.579202667879339e-5
allele num: 13194
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10714
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.381415e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.69e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.634e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.74e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.203e0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16284
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.50140056022409e-4
allele num: 8568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66184
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.556714e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.149999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.37e-1

FS
type: SiteQuality
SIO_000300: 1.602e0

QD
type: SiteQuality
SIO_000300: 1.047e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.464e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11402
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16366
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506568639267205e-5
allele num: 66376
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.560258e6

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.8e-1

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.39e-1

FS
type: SiteQuality
SIO_000300: 9.12e-1

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.087168249330411e-5
allele num: 16428
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8594
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66490
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.271e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.951e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.562662e6

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

African
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allele count: 3
allele frequency: 3.066230580539657e-4
allele num: 9784
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.563472e6

ReadPosRankSum
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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MQ
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.055e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502900598154438e-5
allele num: 66538
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.298e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.231e0

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.721e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.66e0

MQRankSum
type: SiteQuality
SIO_000300: -7.65e-1

DP
type: SiteQuality
SIO_000300: 1.564218e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.2e0

GenotypeQuality
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variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21580547112462e-4
allele num: 16450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66548
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.03e-1

DP
type: SiteQuality
SIO_000300: 1.564432e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.19e-1

BaseQRankSum
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SIO_000300: 2.46e0

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.626e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.134e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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Other
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allele frequency: 0.0e0
allele num: 898
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.076072426783327e-5
allele num: 16458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

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

European (Finnish)
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allele count: 1
allele frequency: 1.515610791148833e-4
allele num: 6598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66558
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.564676e6

FS
type: SiteQuality
SIO_000300: 5.354e0

MQRankSum
type: SiteQuality
SIO_000300: 2.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.69e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.397e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 5.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502042778178322e-5
allele num: 66576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.7e0

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.38e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.98e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.53e-1

QD
type: SiteQuality
SIO_000300: 1.185e1

DP
type: SiteQuality
SIO_000300: 1.56553e6

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

Latino
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allele count: 2
allele frequency: 1.747335313646689e-4
allele num: 11446
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 9.58e0

DP
type: SiteQuality
SIO_000300: 1.565645e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.651e0

FS
type: SiteQuality
SIO_000300: 2.651e0

VQSLOD
type: SiteQuality
SIO_000300: -4.794e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.91e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.83e0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503397678753984e-5
allele num: 66516
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11434
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9790
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.287e0

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

MQ
type: SiteQuality
SIO_000300: 5.927e1

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 9.69e-1

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

Latino
type: Population
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allele frequency: 0.0e0
allele num: 11418
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.090133982947625e-5
allele num: 16420
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66468
num of homozygotes: 0

Other
type: Population
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 3.2e-1

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.562701e6

GenotypeQuality
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variant carriers: 0

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

Latino
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allele frequency: 3.502626970227671e-4
allele num: 11420
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66466
num of homozygotes: 0

European (Finnish)
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allele num: 6588
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East Asian
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num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
type: Population
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MQ
type: SiteQuality
SIO_000300: 5.937e1

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504619180885318e-5
allele num: 66462
num of homozygotes: 0

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e-1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
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MQRankSum
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DP
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ClippingRankSum
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QD
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3910
bin: 9.75e1
variant carriers: 20

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

GenotypeQuality
all individuals: 524
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4741
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16286
num of homozygotes: 0

African
type: Population
allele count: 20
allele frequency: 2.04582651391162e-3
allele num: 9776
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66306
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.44e-1

FS
type: SiteQuality
SIO_000300: 1.589e0

VQSLOD
type: SiteQuality
SIO_000300: 3.69e0

DP
type: SiteQuality
SIO_000300: 1.555101e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

QD
type: SiteQuality
SIO_000300: 1.283e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e-1

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508295625942685e-5
allele num: 66300
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.913e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.41e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.071e-1

DP
type: SiteQuality
SIO_000300: 1.552586e6

QD
type: SiteQuality
SIO_000300: 9.380000000000001e0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 3932
bin: 9.75e1
variant carriers: 36

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16168
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66164
num of homozygotes: 0

East Asian
type: Population
allele count: 37
allele frequency: 4.320411022886501e-3
allele num: 8564
num of homozygotes: 1

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.23e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.97e-1

DP
type: SiteQuality
SIO_000300: 1.539467e6

FS
type: SiteQuality
SIO_000300: 6.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

QD
type: SiteQuality
SIO_000300: 1.51e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.26e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeQuality
all individuals: 43
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1017
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4505
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1071
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.051282051282051e-4
allele num: 9750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16060
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11360
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

QD
type: SiteQuality
SIO_000300: 1.478e1

DP
type: SiteQuality
SIO_000300: 1.506837e6

MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

FS
type: SiteQuality
SIO_000300: 2.948e0

VQSLOD
type: SiteQuality
SIO_000300: 1.76e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.15e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-2

GenotypeQuality
all individuals: 1106
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1405
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4359
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3901
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 99
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2762
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1014
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9740
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.242976651267325e-5
allele num: 16018
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.518648838845883e-4
allele num: 8526
num of homozygotes: 1

QD
type: SiteQuality
SIO_000300: 1.897e1

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.06e-1

MQ
type: SiteQuality
SIO_000300: 5.923e1

FS
type: SiteQuality
SIO_000300: 8.207000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.39e-2

VQSLOD
type: SiteQuality
SIO_000300: -8.475e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.97e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.06e-1

DP
type: SiteQuality
SIO_000300: 1.485179e6

GenotypeQuality
all individuals: 190
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1448
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1223
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 2889
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2879
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65804
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9736
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.171783454417624e-4
allele num: 8534
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15968
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 9.744999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.472e0

MQRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.482012e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

QD
type: SiteQuality
SIO_000300: 1.391e1

GenotypeQuality
all individuals: 23972
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3720
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1021
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3901
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1587
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2157
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11320
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.356470887363335e-5
allele num: 15732
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65308
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.025e1

VQSLOD
type: SiteQuality
SIO_000300: 2.24e0

QD
type: SiteQuality
SIO_000300: 1.557e1

DP
type: SiteQuality
SIO_000300: 1.473796e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

FS
type: SiteQuality
SIO_000300: 1.452e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.89e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.04e-1

GenotypeQuality
all individuals: 84
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1021
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 4551
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3883
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4242
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2308
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11320
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.138952164009112e-3
allele num: 878
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8456
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15732
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65308
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.26e-1

FS
type: SiteQuality
SIO_000300: 1.452e0

QD
type: SiteQuality
SIO_000300: 1.557e1

MQRankSum
type: SiteQuality
SIO_000300: -1.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.04e-1

DP
type: SiteQuality
SIO_000300: 1.473796e6

MQ
type: SiteQuality
SIO_000300: 6.025e1

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 55
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 142
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 396
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 609
bin: 6.75e1
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GenotypeQuality
all individuals: 200
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5637
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 474
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5104
num of homozygotes: 0

European (Finnish)
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: 286
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.401360544217687e-3
allele num: 882
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 196
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.14e1

DP
type: SiteQuality
SIO_000300: 2.07987e5

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.091e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.21e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.142e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.8e-2

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1991
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 164
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.321262766945218e-4
allele num: 4308
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5044
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.560999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQ
type: SiteQuality
SIO_000300: 5.747e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.591e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.419999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.81642e5

QD
type: SiteQuality
SIO_000300: 7.63e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 28

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 7.936507936507936e-3
allele num: 252
num of homozygotes: 0

African
type: Population
allele count: 27
allele frequency: 3.191489361702127e-2
allele num: 846
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4662
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4250
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1598
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

FS
type: SiteQuality
SIO_000300: 1.112e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.44e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

DP
type: SiteQuality
SIO_000300: 1.79349e5

VQSLOD
type: SiteQuality
SIO_000300: 2.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.46e-1

QD
type: SiteQuality
SIO_000300: 1.464e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 393
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 252
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1598
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.797e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.78382e5

FS
type: SiteQuality
SIO_000300: 1.125e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.93e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.006e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 73
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4128
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 250
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 324
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1598
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 148
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.11e-2

DP
type: SiteQuality
SIO_000300: 1.79608e5

QD
type: SiteQuality
SIO_000300: 1.295e1

VQSLOD
type: SiteQuality
SIO_000300: 3.62e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 922
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4038
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 262
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 3.128911138923655e-4
allele num: 3196
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.145e1

MQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

FS
type: SiteQuality
SIO_000300: 3.424e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.76e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.408e0

DP
type: SiteQuality
SIO_000300: 1.91772e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.468e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 982
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4144
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 4.273504273504274e-4
allele num: 2340
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 288
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-2

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.20012e5

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4188
num of homozygotes: 0

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

Other
type: Population
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num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 9.6e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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SIO_000300: 7.27e-1

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

South Asian
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allele count: 0
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allele num: 2166
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 1008
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4284
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.72e-1

MQ
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
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FS
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SIO_000300: 0.0e0

ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -7.95e-2

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.33768e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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