6-131971142-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971142
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971142
    reference: chr 6
allele count: 3
allele frequency: 2.476350849388341e-5
allele num: 121146
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.155-25G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.53-25G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*119-25G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.53-25G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.155-25G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.155-25G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*123-25G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.77-25G>A
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6556
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6812
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50459
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-131971145-CCCTATT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971145
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971139
    reference: chr 6
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*123-21_*123-16delCCTATT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.155-21_155-16delCCTATT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.155-21_155-16delCCTATT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.77-21_77-16delCCTATT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.155-21_155-16delCCTATT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.53-21_53-16delCCTATT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.53-21_53-16delCCTATT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*119-21_*119-16delCCTATT
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6556
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6811
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50464
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: CCCTATT
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum

6-131971147-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971147
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971146
    reference: chr 6
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.155-19delT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*119-19delT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*123-19delT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.53-19delT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.53-19delT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.155-19delT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.155-19delT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.77-19delT
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2674
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6557
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6811
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2962
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: CT
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP

6-131971149-ATTTCC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971149
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971144
    reference: chr 6
allele count: 1
allele frequency: 8.250416646040625e-6
allele num: 121206
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*119-14_*119-10delCCTTT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.77-14_77-10delCCTTT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.155-14_155-10delCCTTT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.155-14_155-10delCCTTT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.53-14_53-10delCCTTT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.155-14_155-10delCCTTT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*123-14_*123-10delCCTTT
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.53-14_53-10delCCTTT
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4640
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6811
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6557
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50465
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3985
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: ATTTCC
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

6-131971158-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971158
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971158
    reference: chr 6
allele count: 21
allele frequency: 1.732101616628175e-4
allele num: 121240
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.53-9A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.155-9A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.77-9A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.155-9A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*123-9A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.155-9A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.53-9A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*119-9A>G
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5741
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4054
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-131971173-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971173
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971173
    reference: chr 6
allele count: 2
allele frequency: 1.648858989579211e-5
allele num: 121296
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*129G>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*125G>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.161G>T
  hgvsp: ENSP00000406261.1:p.Cys54Phe
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.161G>T
  hgvsp: ENSP00000350265.3:p.Cys54Phe
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.83G>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.161G>T
  hgvsp: ENSP00000350964.5:p.Cys54Phe
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.59G>T
  hgvsp: ENSP00000399269.2:p.Cys20Phe
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.59G>T
  hgvsp: ENSP00000440810.1:p.Cys20Phe
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5741
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 986
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Cys54Phe
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

6-131971174-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971174
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971174
    reference: chr 6
allele count: 3
allele frequency: 2.47320692497939e-5
allele num: 121300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.162C>T
  hgvsp: ENST00000358229.5:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*126C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.162C>T
  hgvsp: ENST00000414305.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.162C>T
  hgvsp: ENST00000357639.3:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.60C>T
  hgvsp: ENST00000543135.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.60C>T
  hgvsp: ENST00000427148.2:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.84C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*130C>T
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6807
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 688
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 986
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Cys54Cys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

6-131971186-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971186
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971186
    reference: chr 6
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*138C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.174C>T
  hgvsp: ENST00000414305.1:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.174C>T
  hgvsp: ENST00000357639.3:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.174C>T
  hgvsp: ENST00000358229.5:c.174C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.96C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*142C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.72C>T
  hgvsp: ENST00000543135.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.72C>T
  hgvsp: ENST00000427148.2:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6136
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5741
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4078
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1433
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50473
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4147
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Cys58Cys
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

6-131971188-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971188
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971188
    reference: chr 6
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.74T>G
  hgvsp: ENSP00000440810.1:p.Phe25Cys
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.176T>G
  hgvsp: ENSP00000350964.5:p.Phe59Cys
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*144T>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*140T>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.176T>G
  hgvsp: ENSP00000406261.1:p.Phe59Cys
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.176T>G
  hgvsp: ENSP00000350265.3:p.Phe59Cys
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.98T>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.74T>G
  hgvsp: ENSP00000399269.2:p.Phe25Cys
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5741
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50473
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Phe59Cys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

6-131971190-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971190
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971190
    reference: chr 6
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.178G>A
  hgvsp: ENSP00000406261.1:p.Asp60Asn
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.76G>A
  hgvsp: ENSP00000440810.1:p.Asp26Asn
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.76G>A
  hgvsp: ENSP00000399269.2:p.Asp26Asn
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*142G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.100G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*146G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.178G>A
  hgvsp: ENSP00000350964.5:p.Asp60Asn
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.178G>A
  hgvsp: ENSP00000350265.3:p.Asp60Asn
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6805
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6555
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5741
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1433
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp60Asn
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ

6-131971192-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971192
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971192
    reference: chr 6
allele count: 2
allele frequency: 1.648424106554134e-5
allele num: 121328
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.78T>C
  hgvsp: ENST00000543135.1:c.78T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.180T>C
  hgvsp: ENST00000414305.1:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*144T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.180T>C
  hgvsp: ENST00000358229.5:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.78T>C
  hgvsp: ENST00000427148.2:c.78T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.180T>C
  hgvsp: ENST00000357639.3:c.180T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*148T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.102T>C
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2780
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4079
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5741
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4143
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp60Asp
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/6-131971197-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971197
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971197
    reference: chr 6
allele count: 3
allele frequency: 2.472350876036327e-5
allele num: 121342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*149C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.185C>A
  hgvsp: ENSP00000350265.3:p.Ser62Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.185C>A
  hgvsp: ENSP00000406261.1:p.Ser62Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.107C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.83C>A
  hgvsp: ENSP00000440810.1:p.Ser28Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.185C>A
  hgvsp: ENSP00000350964.5:p.Ser62Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*153C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.83C>A
  hgvsp: ENSP00000399269.2:p.Ser28Ter
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 987
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1428
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser62Ter
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

6-131971197-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971197
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971197
    reference: chr 6
allele count: 15
allele frequency: 1.236175438018163e-4
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.83C>T
  hgvsp: ENSP00000440810.1:p.Ser28Leu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*149C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*153C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.107C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.185C>T
  hgvsp: ENSP00000350964.5:p.Ser62Leu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.185C>T
  hgvsp: ENSP00000350265.3:p.Ser62Leu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.185C>T
  hgvsp: ENSP00000406261.1:p.Ser62Leu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.83C>T
  hgvsp: ENSP00000399269.2:p.Ser28Leu
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4088
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50476
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser62Leu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

6-131971198-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971198
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971198
    reference: chr 6
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.186A>G
  hgvsp: ENST00000357639.3:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.186A>G
  hgvsp: ENST00000414305.1:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*150A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.108A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.186A>G
  hgvsp: ENST00000358229.5:c.186A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.84A>G
  hgvsp: ENST00000427148.2:c.84A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.84A>G
  hgvsp: ENST00000543135.1:c.84A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*154A>G
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1696
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6807
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2412
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser62Ser
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

6-131971199-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971199
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971199
    reference: chr 6
allele count: 2
allele frequency: 1.648261084555794e-5
allele num: 121340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*151T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.109T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.187T>C
  hgvsp: ENSP00000406261.1:p.Phe63Leu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.85T>C
  hgvsp: ENSP00000440810.1:p.Phe29Leu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*155T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.187T>C
  hgvsp: ENSP00000350964.5:p.Phe63Leu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.187T>C
  hgvsp: ENSP00000350265.3:p.Phe63Leu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.85T>C
  hgvsp: ENSP00000399269.2:p.Phe29Leu
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6553
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe63Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

6-131971204-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971204
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971204
    reference: chr 6
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.114A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*160A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.90A>G
  hgvsp: ENST00000543135.1:c.90A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.192A>G
  hgvsp: ENST00000414305.1:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.90A>G
  hgvsp: ENST00000427148.2:c.90A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.192A>G
  hgvsp: ENST00000357639.3:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.192A>G
  hgvsp: ENST00000358229.5:c.192A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*156A>G
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2782
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6552
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50475
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1438
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg64Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS

http://identifiers.org/exac.variant/6-131971207-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971207
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971207
    reference: chr 6
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*159A>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.195A>C
  hgvsp: ENST00000358229.5:c.195A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.195A>C
  hgvsp: ENST00000357639.3:c.195A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*163A>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.195A>C
  hgvsp: ENST00000414305.1:c.195A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.93A>C
  hgvsp: ENST00000427148.2:c.93A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.93A>C
  hgvsp: ENST00000543135.1:c.93A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.117A>C
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6551
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4152
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50476
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gly65Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

6-131971220-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971220
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971220
    reference: chr 6
allele count: 4
allele frequency: 3.296467834715103e-5
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.106C>T
  hgvsp: ENSP00000399269.2:p.Arg36Trp
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*176C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.208C>T
  hgvsp: ENSP00000406261.1:p.Arg70Trp
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.106C>T
  hgvsp: ENSP00000440810.1:p.Arg36Trp
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.130C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*172C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.208C>T
  hgvsp: ENSP00000350265.3:p.Arg70Trp
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.208C>T
  hgvsp: ENSP00000350964.5:p.Arg70Trp
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5740
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6551
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4641
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4090
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 738
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4155
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg70Trp
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

6-131971221-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971221
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971221
    reference: chr 6
allele count: 16
allele frequency: 1.318391562294001e-4
allele num: 121360
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.209G>A
  hgvsp: ENSP00000406261.1:p.Arg70Gln
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.107G>A
  hgvsp: ENSP00000399269.2:p.Arg36Gln
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.131G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*173G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*177G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.209G>A
  hgvsp: ENSP00000350265.3:p.Arg70Gln
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.209G>A
  hgvsp: ENSP00000350964.5:p.Arg70Gln
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.107G>A
  hgvsp: ENSP00000440810.1:p.Arg36Gln
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6801
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 9.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4164
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg70Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

6-131971224-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971224
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971224
    reference: chr 6
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.134G>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.212G>T
  hgvsp: ENSP00000406261.1:p.Cys71Phe
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.110G>T
  hgvsp: ENSP00000399269.2:p.Cys37Phe
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*180G>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.212G>T
  hgvsp: ENSP00000350265.3:p.Cys71Phe
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.110G>T
  hgvsp: ENSP00000440810.1:p.Cys37Phe
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*176G>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.212G>T
  hgvsp: ENSP00000350964.5:p.Cys71Phe
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2788
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6547
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4091
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2852
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1000
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys71Phe
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

6-131971230-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971230
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971230
    reference: chr 6
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.218T>A
  hgvsp: ENSP00000350265.3:p.Val73Glu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.218T>A
  hgvsp: ENSP00000406261.1:p.Val73Glu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*182T>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.116T>A
  hgvsp: ENSP00000399269.2:p.Val39Glu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.218T>A
  hgvsp: ENSP00000350964.5:p.Val73Glu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*186T>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.116T>A
  hgvsp: ENSP00000440810.1:p.Val39Glu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.140T>A
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6547
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4092
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4167
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val73Glu
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: T
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

6-131971243-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971243
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971243
    reference: chr 6
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.129C>G
  hgvsp: ENSP00000440810.1:p.Asp43Glu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*199C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.231C>G
  hgvsp: ENSP00000406261.1:p.Asp77Glu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.153C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.129C>G
  hgvsp: ENSP00000399269.2:p.Asp43Glu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.231C>G
  hgvsp: ENSP00000350265.3:p.Asp77Glu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.231C>G
  hgvsp: ENSP00000350964.5:p.Asp77Glu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*195C>G
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6803
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6547
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4092
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50477
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp77Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/6-131971244-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971244
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971244
    reference: chr 6
allele count: 5
allele frequency: 4.119294776734223e-5
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.154C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*196C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.130C>A
  hgvsp: ENST00000543135.1:c.130C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.130C>A
  hgvsp: ENST00000427148.2:c.130C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.232C>A
  hgvsp: ENST00000357639.3:c.232C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.232C>A
  hgvsp: ENST00000358229.5:c.232C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*200C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.232C>A
  hgvsp: ENST00000414305.1:c.232C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6118
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 999
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4167
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg78Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

6-131971244-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971244
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971244
    reference: chr 6
allele count: 133
allele frequency: 1.095732410611303e-3
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.154C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.130C>T
  hgvsp: ENSP00000440810.1:p.Arg44Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.130C>T
  hgvsp: ENSP00000399269.2:p.Arg44Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.232C>T
  hgvsp: ENSP00000350964.5:p.Arg78Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*200C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*196C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.232C>T
  hgvsp: ENSP00000350265.3:p.Arg78Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.232C>T
  hgvsp: ENSP00000406261.1:p.Arg78Ter
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4211
  bin: 9.75e1
  variant carriers: 125
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6118
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1453
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4167
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg78Ter
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

6-131971245-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971245
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971245
    reference: chr 6
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.233G>A
  hgvsp: ENSP00000350265.3:p.Arg78Gln
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.155G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.131G>A
  hgvsp: ENSP00000399269.2:p.Arg44Gln
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*197G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.131G>A
  hgvsp: ENSP00000440810.1:p.Arg44Gln
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.233G>A
  hgvsp: ENSP00000350964.5:p.Arg78Gln
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*201G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.233G>A
  hgvsp: ENSP00000406261.1:p.Arg78Gln
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6537
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2423
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6786
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4140
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg78Gln
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

6-131971259-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971259
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971259
    reference: chr 6
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*215T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*211T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.145T>C
  hgvsp: ENSP00000399269.2:p.Trp49Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.145T>C
  hgvsp: ENSP00000440810.1:p.Trp49Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.169T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.247T>C
  hgvsp: ENSP00000406261.1:p.Trp83Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.247T>C
  hgvsp: ENSP00000350265.3:p.Trp83Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.247T>C
  hgvsp: ENSP00000350964.5:p.Trp83Arg
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4143
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6536
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6786
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Trp83Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

6-131971260-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971260
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971260
    reference: chr 6
allele count: 15
allele frequency: 1.235747709747578e-4
allele num: 121384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.170G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*212G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.146G>A
  hgvsp: ENSP00000399269.2:p.Trp49Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.248G>A
  hgvsp: ENSP00000350964.5:p.Trp83Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.248G>A
  hgvsp: ENSP00000406261.1:p.Trp83Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.146G>A
  hgvsp: ENSP00000440810.1:p.Trp49Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.248G>A
  hgvsp: ENSP00000350265.3:p.Trp83Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*216G>A
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4153
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4170
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1454
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Trp83Ter
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/6-131971275-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971275
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971275
    reference: chr 6
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.185C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.263C>A
  hgvsp: ENSP00000350964.5:p.Thr88Asn
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.161C>A
  hgvsp: ENSP00000399269.2:p.Thr54Asn
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.161C>A
  hgvsp: ENSP00000440810.1:p.Thr54Asn
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*231C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.263C>A
  hgvsp: ENSP00000350265.3:p.Thr88Asn
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.263C>A
  hgvsp: ENSP00000406261.1:p.Thr88Asn
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*227C>A
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6786
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4147
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50484
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Thr88Asn
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

6-131971291-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971291
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971291
    reference: chr 6
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.277+2T>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.175+2T>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.277+2T>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.175+2T>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*241+2T>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.277+2T>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*245+2T>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.199+2T>A
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2916
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6537
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4148
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6786
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4146
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: c.277+2T>A
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

6-131971294-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971294
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971294
    reference: chr 6
allele count: 6
allele frequency: 4.943886883868097e-5
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.175+5G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.175+5G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*245+5G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*241+5G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.199+5G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.277+5G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.277+5G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.277+5G>A
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6786
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2424
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6537
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1449
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50484
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
hgvs: c.277+5G>A
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP

6-131971296-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971296
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971296
    reference: chr 6
allele count: 733
allele frequency: 6.039781809792192e-3
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.277+7G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.277+7G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*245+7G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.199+7G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*241+7G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.277+7G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.175+7G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.175+7G>A
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6739
  bin: 5.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 2792
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6512
  bin: 5.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 7.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 6076
  bin: 4.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 5714
  bin: 6.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2813
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 7.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4627
  bin: 6.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4582
  bin: 9.75e1
  variant carriers: 464
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 8.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 4.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 8.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 4044
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: c.277+7G>A
num of homozygotes: 9
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum

6-131971300-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971300
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971300
    reference: chr 6
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*241+11T>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.277+11T>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.175+11T>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.175+11T>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.277+11T>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*245+11T>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.277+11T>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.199+11T>G
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4646
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4254
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6074
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5709
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 973
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

6-131971304-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971304
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971304
    reference: chr 6
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.277+15A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*241+15A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.175+15A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*245+15A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.277+15A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.199+15A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.175+15A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.277+15A>G
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6728
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6506
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5709
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4128
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50510
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

6-131971314-T-TTAGCATGTTGCTTGTGTTACTA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971314
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971336
    reference: chr 6
allele count: 1
allele frequency: 8.241169586787756e-6
allele num: 121342
alternate allele: TTAGCATGTTGCTTGTGTTACTA
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4254
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5709
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2841
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1433
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 989
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

6-131971317-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971317
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971317
    reference: chr 6
allele count: 7
allele frequency: 5.769294168067781e-5
allele num: 121332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.199+28G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*241+28G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*245+28G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.175+28G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.277+28G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.277+28G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.277+28G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.175+28G>A
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4259
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3521
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6727
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4645
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 728
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

6-131971321-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971321
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971321
    reference: chr 6
allele count: 2
allele frequency: 1.648478454386601e-5
allele num: 121324
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*245+32G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.277+32G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.175+32G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*241+32G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.277+32G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.277+32G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.199+32G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.175+32G>A
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4257
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6726
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1397
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3799
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

6-131971334-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971334
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971334
    reference: chr 6
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*241+45C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.175+45C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*245+45C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.175+45C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.199+45C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.277+45C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.277+45C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.277+45C>T
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6069
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4257
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6725
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3360
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1301
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 966
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3043
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

6-131971338-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131971338
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131971338
    reference: chr 6
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*245+49T>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.277+49T>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*241+49T>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.175+49T>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.199+49T>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.175+49T>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.277+49T>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.277+49T>A
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6068
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6504
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4644
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4257
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6725
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

6-131973636-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973636
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973636
    reference: chr 6
allele count: 15
allele frequency: 1.246613367019597e-4
allele num: 120326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.278-46A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*246-46A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*242-46A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.200-46A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.278-46A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.278-46A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.176-46A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.176-46A>G
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4972
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6977
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7131
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4352
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1600
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2432
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

6-131973639-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973639
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973639
    reference: chr 6
allele count: 6
allele frequency: 4.984465083822088e-5
allele num: 120374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*246-43C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.176-43C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*242-43C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.278-43C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.200-43C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.176-43C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.278-43C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.278-43C>T
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6979
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4369
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5978
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4973
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7129
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2950
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2546
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2453
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

6-131973640-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973640
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973640
    reference: chr 6
allele count: 1
allele frequency: 8.303440945927993e-6
allele num: 120432
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.176-42T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*242-42T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.200-42T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.278-42T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.176-42T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.278-42T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*246-42T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.278-42T>C
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6981
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5979
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4973
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6060
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2268
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1451
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2585
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2468
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1613
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-131973646-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973646
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973646
    reference: chr 6
allele count: 2
allele frequency: 1.657193046417977e-5
allele num: 120686
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.278-36C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*246-36C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.176-36C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*242-36C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.200-36C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.278-36C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.278-36C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.176-36C>G
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6060
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4637
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5994
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4973
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2971
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP

6-131973656-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973656
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973656
    reference: chr 6
allele count: 18
allele frequency: 1.487578717707145e-4
allele num: 121002
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.278-26C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*242-26C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*246-26C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.176-26C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.278-26C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.176-26C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.278-26C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.200-26C>G
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6060
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1653
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7129
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2982
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5966
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1530
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2753
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/6-131973659-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973659
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973659
    reference: chr 6
allele count: 2
allele frequency: 1.65188231990353e-5
allele num: 121074
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.278-23A>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*242-23A>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.176-23A>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.278-23A>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.200-23A>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.176-23A>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*246-23A>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.278-23A>C
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4972
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5776
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2566
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6071
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2779
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD

http://identifiers.org/exac.variant/6-131973672-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973672
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973672
    reference: chr 6
allele count: 3
allele frequency: 2.474675817467912e-5
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.278-10C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.176-10C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*246-10C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*242-10C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.278-10C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.200-10C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.278-10C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.176-10C>A
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4970
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1543
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40088
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

6-131973672-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973672
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973672
    reference: chr 6
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.176-10C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*242-10C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*246-10C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.278-10C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.278-10C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.176-10C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.200-10C>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.278-10C>G
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4970
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2631
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2570
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1543
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

6-131973672-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973672
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973672
    reference: chr 6
allele count: 13
allele frequency: 1.072359520902762e-4
allele num: 121228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.200-10C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.176-10C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.278-10C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*246-10C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*242-10C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.176-10C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.278-10C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.278-10C>T
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1144
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6010
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7134
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4970
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2631
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

6-131973673-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973673
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973673
    reference: chr 6
allele count: 111
allele frequency: 9.155545291080354e-4
allele num: 121238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*246-9G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.200-9G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.278-9G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.278-9G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*242-9G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.176-9G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.278-9G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.176-9G>A
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4969
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6053
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6986
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6007
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5386
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 9.75e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5774
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7123
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6186
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2834
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1636
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40109
  bin: 9.75e1
  variant carriers: 110
num of homozygotes: 1
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: QD

6-131973678-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973678
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973678
    reference: chr 6
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*242-4A>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.176-4A>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.200-4A>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.176-4A>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.278-4A>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.278-4A>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*246-4A>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.278-4A>T
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4980
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2269
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6067
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5397
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7133
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1638
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
hgvs: c.278-4A>T
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS

6-131973680-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973680
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973680
    reference: chr 6
allele count: 49
allele frequency: 4.040837195494054e-4
allele num: 121262
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*242-2A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.176-2A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.278-2A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*246-2A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.200-2A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.278-2A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.278-2A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.176-2A>G
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2284
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5395
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5019
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7135
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6012
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2855
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2629
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 8.75e1
  variant carriers: 0
hgvs: c.278-2A>G
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP

6-131973684-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973684
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973684
    reference: chr 6
allele count: 18
allele frequency: 1.484168865435356e-4
allele num: 121280
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.280C>T
  hgvsp: ENSP00000406261.1:p.Arg94Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.280C>T
  hgvsp: ENSP00000350265.3:p.Arg94Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.280C>T
  hgvsp: ENSP00000350964.5:p.Arg94Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*248C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.178C>T
  hgvsp: ENSP00000399269.2:p.Arg60Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*244C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.178C>T
  hgvsp: ENSP00000440810.1:p.Arg60Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.202C>T
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 7138
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4984
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6022
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5750
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6995
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2994
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2861
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6220
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg94Ter
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-131973685-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973685
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973685
    reference: chr 6
allele count: 22
allele frequency: 1.813924342864681e-4
allele num: 121284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.203G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*249G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.179G>A
  hgvsp: ENSP00000440810.1:p.Arg60Gln
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.281G>A
  hgvsp: ENSP00000406261.1:p.Arg94Gln
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.281G>A
  hgvsp: ENSP00000350265.3:p.Arg94Gln
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.281G>A
  hgvsp: ENSP00000350964.5:p.Arg94Gln
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.179G>A
  hgvsp: ENSP00000399269.2:p.Arg60Gln
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*245G>A
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6060
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 9.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1559
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2996
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg94Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

6-131973690-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973690
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973690
    reference: chr 6
allele count: 2
allele frequency: 1.648777431534517e-5
allele num: 121302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.208T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.184T>C
  hgvsp: ENSP00000440810.1:p.Trp62Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.286T>C
  hgvsp: ENSP00000406261.1:p.Trp96Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.184T>C
  hgvsp: ENSP00000399269.2:p.Trp62Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.286T>C
  hgvsp: ENSP00000350265.3:p.Trp96Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*250T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*254T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.286T>C
  hgvsp: ENSP00000350964.5:p.Trp96Arg
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1139
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3798
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2640
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40074
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Trp96Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

6-131973691-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973691
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973691
    reference: chr 6
allele count: 10
allele frequency: 8.243615319934711e-5
allele num: 121306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*251G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.185G>A
  hgvsp: ENSP00000440810.1:p.Trp62Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.287G>A
  hgvsp: ENSP00000350265.3:p.Trp96Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.209G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.287G>A
  hgvsp: ENSP00000350964.5:p.Trp96Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*255G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.185G>A
  hgvsp: ENSP00000399269.2:p.Trp62Ter
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.287G>A
  hgvsp: ENSP00000406261.1:p.Trp96Ter
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2479
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5759
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3799
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4985
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6258
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Trp96Ter
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

6-131973700-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973700
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973700
    reference: chr 6
allele count: 60
allele frequency: 4.945353840067257e-4
allele num: 121326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.194A>G
  hgvsp: ENSP00000440810.1:p.Asn65Ser
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.296A>G
  hgvsp: ENSP00000350265.3:p.Asn99Ser
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.296A>G
  hgvsp: ENSP00000406261.1:p.Asn99Ser
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.194A>G
  hgvsp: ENSP00000399269.2:p.Asn65Ser
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.218A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.296A>G
  hgvsp: ENSP00000350964.5:p.Asn99Ser
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*260A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*264A>G
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6995
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2313
  bin: 9.75e1
  variant carriers: 55
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2643
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2997
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn99Ser
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: A
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

6-131973708-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973708
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973708
    reference: chr 6
allele count: 3
allele frequency: 2.472676920033628e-5
allele num: 121326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.202C>T
  hgvsp: ENSP00000399269.2:p.Arg68Cys
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.202C>T
  hgvsp: ENSP00000440810.1:p.Arg68Cys
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*268C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.226C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.304C>T
  hgvsp: ENSP00000350964.5:p.Arg102Cys
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.304C>T
  hgvsp: ENSP00000350265.3:p.Arg102Cys
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*272C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.304C>T
  hgvsp: ENSP00000406261.1:p.Arg102Cys
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4983
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2643
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2862
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg102Cys
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

6-131973709-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973709
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973709
    reference: chr 6
allele count: 6
allele frequency: 4.945190801945108e-5
allele num: 121330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.305G>A
  hgvsp: ENSP00000350964.5:p.Arg102His
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.305G>A
  hgvsp: ENSP00000406261.1:p.Arg102His
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*273G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*269G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.305G>A
  hgvsp: ENSP00000350265.3:p.Arg102His
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.227G>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.203G>A
  hgvsp: ENSP00000440810.1:p.Arg68His
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.203G>A
  hgvsp: ENSP00000399269.2:p.Arg68His
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2863
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2569
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg102His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

6-131973712-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973712
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973712
    reference: chr 6
allele count: 2
allele frequency: 1.648342591524222e-5
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.308G>T
  hgvsp: ENSP00000350265.3:p.Cys103Phe
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.206G>T
  hgvsp: ENSP00000440810.1:p.Cys69Phe
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*272G>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.308G>T
  hgvsp: ENSP00000350964.5:p.Cys103Phe
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*276G>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.308G>T
  hgvsp: ENSP00000406261.1:p.Cys103Phe
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.230G>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.206G>T
  hgvsp: ENSP00000399269.2:p.Cys69Phe
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys103Phe
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

6-131973719-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973719
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973719
    reference: chr 6
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*283G>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.315G>T
  hgvsp: ENSP00000350964.5:p.Glu105Asp
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.213G>T
  hgvsp: ENSP00000440810.1:p.Glu71Asp
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.315G>T
  hgvsp: ENSP00000350265.3:p.Glu105Asp
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.315G>T
  hgvsp: ENSP00000406261.1:p.Glu105Asp
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.213G>T
  hgvsp: ENSP00000399269.2:p.Glu71Asp
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.237G>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*279G>T
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2483
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2571
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6278
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Glu105Asp
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-131973721-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973721
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973721
    reference: chr 6
allele count: 46
allele frequency: 3.791000494478325e-4
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.317C>A
  hgvsp: ENSP00000350265.3:p.Thr106Asn
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.239C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.317C>A
  hgvsp: ENSP00000350964.5:p.Thr106Asn
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.317C>A
  hgvsp: ENSP00000406261.1:p.Thr106Asn
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*281C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.215C>A
  hgvsp: ENSP00000399269.2:p.Thr72Asn
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.215C>A
  hgvsp: ENSP00000440810.1:p.Thr72Asn
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*285C>A
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3797
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2306
  bin: 9.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6282
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2643
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr106Asn
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

6-131973723-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973723
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973723
    reference: chr 6
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.319A>G
  hgvsp: ENSP00000406261.1:p.Arg107Gly
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*287A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.217A>G
  hgvsp: ENSP00000440810.1:p.Arg73Gly
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.319A>G
  hgvsp: ENSP00000350265.3:p.Arg107Gly
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.319A>G
  hgvsp: ENSP00000350964.5:p.Arg107Gly
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.217A>G
  hgvsp: ENSP00000399269.2:p.Arg73Gly
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*283A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.241A>G
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6997
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6063
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6285
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2864
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg107Gly
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/6-131973737-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973737
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973737
    reference: chr 6
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.255C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.333C>A
  hgvsp: ENSP00000350964.5:p.Ser111Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.333C>A
  hgvsp: ENSP00000350265.3:p.Ser111Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*301C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*297C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.333C>A
  hgvsp: ENSP00000406261.1:p.Ser111Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.231C>A
  hgvsp: ENSP00000440810.1:p.Ser77Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.231C>A
  hgvsp: ENSP00000399269.2:p.Ser77Arg
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6064
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2646
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1569
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser111Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD

6-131973739-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973739
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973739
    reference: chr 6
allele count: 6
allele frequency: 4.944131316127757e-5
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.335T>C
  hgvsp: ENSP00000406261.1:p.Leu112Pro
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*303T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.257T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.233T>C
  hgvsp: ENSP00000399269.2:p.Leu78Pro
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.335T>C
  hgvsp: ENSP00000350964.5:p.Leu112Pro
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*299T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.335T>C
  hgvsp: ENSP00000350265.3:p.Leu112Pro
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.233T>C
  hgvsp: ENSP00000440810.1:p.Leu78Pro
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6063
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40082
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 2860
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1571
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2644
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu112Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS

6-131973771-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973771
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973771
    reference: chr 6
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.289A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.265A>G
  hgvsp: ENSP00000399269.2:p.Lys89Glu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.367A>G
  hgvsp: ENSP00000350964.5:p.Lys123Glu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.367A>G
  hgvsp: ENSP00000350265.3:p.Lys123Glu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.265A>G
  hgvsp: ENSP00000440810.1:p.Lys89Glu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*335A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.367A>G
  hgvsp: ENSP00000406261.1:p.Lys123Glu
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*331A>G
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6025
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys123Glu
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

6-131973772-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973772
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973772
    reference: chr 6
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.266A>G
  hgvsp: ENSP00000399269.2:p.Lys89Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.368A>G
  hgvsp: ENSP00000350265.3:p.Lys123Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.266A>G
  hgvsp: ENSP00000440810.1:p.Lys89Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.368A>G
  hgvsp: ENSP00000406261.1:p.Lys123Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*332A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*336A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.368A>G
  hgvsp: ENSP00000350964.5:p.Lys123Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.290A>G
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6025
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2861
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6266
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2644
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys123Arg
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

6-131973773-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973773
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973773
    reference: chr 6
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.369A>G
  hgvsp: ENST00000357639.3:c.369A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.369A>G
  hgvsp: ENST00000358229.5:c.369A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.267A>G
  hgvsp: ENST00000543135.1:c.267A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.291A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.267A>G
  hgvsp: ENST00000427148.2:c.267A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*333A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.369A>G
  hgvsp: ENST00000414305.1:c.369A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*337A>G
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6027
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1565
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6265
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys123Lys
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum

6-131973776-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973776
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973776
    reference: chr 6
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.294T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.270T>C
  hgvsp: ENST00000543135.1:c.270T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.372T>C
  hgvsp: ENST00000414305.1:c.372T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.270T>C
  hgvsp: ENST00000427148.2:c.270T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.372T>C
  hgvsp: ENST00000358229.5:c.372T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*336T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*340T>C
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.372T>C
  hgvsp: ENST00000357639.3:c.372T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2488
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6025
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1564
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40079
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp124Asp
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/6-131973784-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973784
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973784
    reference: chr 6
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*344C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.380C>A
  hgvsp: ENSP00000350964.5:p.Ala127Asp
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.380C>A
  hgvsp: ENSP00000406261.1:p.Ala127Asp
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.380C>A
  hgvsp: ENSP00000350265.3:p.Ala127Asp
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.278C>A
  hgvsp: ENSP00000440810.1:p.Ala93Asp
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*348C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.302C>A
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.278C>A
  hgvsp: ENSP00000399269.2:p.Ala93Asp
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2995
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2644
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala127Asp
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

6-131973788-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973788
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973788
    reference: chr 6
allele count: 2
allele frequency: 1.648288252649623e-5
allele num: 121338
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*352C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.384C>T
  hgvsp: ENST00000414305.1:c.384C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.384C>T
  hgvsp: ENST00000358229.5:c.384C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.282C>T
  hgvsp: ENST00000543135.1:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.282C>T
  hgvsp: ENST00000427148.2:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*348C>T
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.384C>T
  hgvsp: ENST00000357639.3:c.384C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.306C>T
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6063
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2857
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp128Asp
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

6-131973790-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973790
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973790
    reference: chr 6
allele count: 2
allele frequency: 1.648233917357551e-5
allele num: 121342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.386A>G
  hgvsp: ENSP00000350265.3:p.Tyr129Cys
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.308A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000408642
  ensembl transcript: ENST00000423831
  gene symbol: ENPP3
  hgvsc: ENST00000423831.1:c.*354A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*350A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.386A>G
  hgvsp: ENSP00000406261.1:p.Tyr129Cys
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.284A>G
  hgvsp: ENSP00000399269.2:p.Tyr95Cys
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.284A>G
  hgvsp: ENSP00000440810.1:p.Tyr95Cys
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.386A>G
  hgvsp: ENSP00000350964.5:p.Tyr129Cys
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3801
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5696
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2860
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr129Cys
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

6-131973793-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 131973793
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 131973793
    reference: chr 6
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350964
  ensembl transcript: ENST00000358229
  gene symbol: ENPP3
  hgvsc: ENST00000358229.5:c.389A>G
  hgvsp: ENSP00000350964.5:p.Lys130Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000440810
  ensembl transcript: ENST00000543135
  gene symbol: ENPP3
  hgvsc: ENST00000543135.1:c.287A>G
  hgvsp: ENSP00000440810.1:p.Lys96Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000415589
  ensembl transcript: ENST00000427707
  gene symbol: ENPP3
  hgvsc: ENST00000427707.1:c.*353A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000154269
  ensembl transcript: ENST00000470930
  gene symbol: ENPP3
  hgvsc: ENST00000470930.1:n.311A>G
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000399269
  ensembl transcript: ENST00000427148
  gene symbol: ENPP3
  hgvsc: ENST00000427148.2:c.287A>G
  hgvsp: ENSP00000399269.2:p.Lys96Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000350265
  ensembl transcript: ENST00000357639
  gene symbol: ENPP3
  hgvsc: ENST00000357639.3:c.389A>G
  hgvsp: ENSP00000350265.3:p.Lys130Arg
  variant of: http://identifiers.org/hgnc/3358
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000154269
  ensembl protein: ENSP00000406261
  ensembl transcript: ENST00000414305
  gene symbol: ENPP3
  hgvsc: ENST00000414305.1:c.389A>G
  hgvsp: ENSP00000406261.1:p.Lys130Arg
  variant of: http://identifiers.org/hgnc/3358
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7144
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys130Arg
num of homozygotes: 0
reference allele: A

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

GenotypeQuality
all individuals: 86
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 662
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1376
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3858
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003093185981561e-5
allele num: 66598
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.505349e6

MQ
type: SiteQuality
SIO_000300: 5.979e1

MQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

FS
type: SiteQuality
SIO_000300: 6.728e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.37e0

QD
type: SiteQuality
SIO_000300: 1.254e1

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.16e-1

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

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3887
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1388
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50105073551486e-5
allele num: 66620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.048e1

DP
type: SiteQuality
SIO_000300: 3.506893e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.23e0

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

QD
type: SiteQuality
SIO_000300: 8.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.820000000000001e-1

FS
type: SiteQuality
SIO_000300: 6.799e0

MQRankSum
type: SiteQuality
SIO_000300: -6.181e0

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

GenotypeQuality
all individuals: 674
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50464
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1144
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3951
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 993
bin: 8.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500960614793468e-5
allele num: 66624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

MQ
type: SiteQuality
SIO_000300: 5.754e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.178e0

MQRankSum
type: SiteQuality
SIO_000300: -2.09e0

VQSLOD
type: SiteQuality
SIO_000300: 4.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 6.27e0

DP
type: SiteQuality
SIO_000300: 3.50745e6

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

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

GenotypeQuality
all individuals: 1145
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 999
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 681
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.918e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

MQ
type: SiteQuality
SIO_000300: 5.67e1

FS
type: SiteQuality
SIO_000300: 8.863e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.022e0

VQSLOD
type: SiteQuality
SIO_000300: -2.845e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.87e0

DP
type: SiteQuality
SIO_000300: 3.507891e6

MQRankSum
type: SiteQuality
SIO_000300: -2.983e0

QD
type: SiteQuality
SIO_000300: 1.56e0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1423
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 984
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50471
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 997
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 20
allele frequency: 1.734906315058987e-3
allele num: 11528
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5004651441947e-5
allele num: 66646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.516e1

MQRankSum
type: SiteQuality
SIO_000300: 4.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

FS
type: SiteQuality
SIO_000300: 1.277e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.16e0

DP
type: SiteQuality
SIO_000300: 3.509948e6

MQ
type: SiteQuality
SIO_000300: 5.972e1

VQSLOD
type: SiteQuality
SIO_000300: 2.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.669999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.77e-1

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

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 998
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50471
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 44
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1146
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4119
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1433
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
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: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

QD
type: SiteQuality
SIO_000300: 1.439e1

DP
type: SiteQuality
SIO_000300: 3.511165e6

FS
type: SiteQuality
SIO_000300: 3.346e0

VQSLOD
type: SiteQuality
SIO_000300: 4.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.318e0

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

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 41
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4123
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1433
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50474
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 998
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.66e-1

QD
type: SiteQuality
SIO_000300: 1.155e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.926e0

MQRankSum
type: SiteQuality
SIO_000300: -3.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

DP
type: SiteQuality
SIO_000300: 3.511394e6

FS
type: SiteQuality
SIO_000300: 5.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.51e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

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

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

GenotypeQuality
all individuals: 1146
bin: 9.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 997
bin: 8.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.429e0

FS
type: SiteQuality
SIO_000300: 7.108e0

MQRankSum
type: SiteQuality
SIO_000300: -1.09e0

QD
type: SiteQuality
SIO_000300: 1.168e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

VQSLOD
type: SiteQuality
SIO_000300: -8.007e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.2e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

DP
type: SiteQuality
SIO_000300: 3.511836e6

GenotypeQuality
all individuals: 4146
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1434
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1147
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 987
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 693
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

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

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

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

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

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

MQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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FS
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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MQ
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SIO_000300: 5.951e1

BaseQRankSum
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SIO_000300: 3.97e0

QD
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SIO_000300: 1.679e1

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: 4.75e1
variant carriers: 0

South Asian
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allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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BaseQRankSum
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DP
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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FS
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QD
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VQSLOD
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MQ
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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

Latino
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allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997961386257345e-5
allele num: 66712
num of homozygotes: 0

African
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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QD
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FS
type: SiteQuality
SIO_000300: 5.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.72e-1

BaseQRankSum
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ClippingRankSum
type: SiteQuality
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VQSLOD
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SIO_000300: 2.35e0

MQRankSum
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InbreedingCoeff
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DP
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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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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

East Asian
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allele count: 3
allele frequency: 3.469812630117973e-4
allele num: 8646
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66718
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South Asian
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VQSLOD
type: SiteQuality
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ReadPosRankSum
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QD
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BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -2.57e-1

ClippingRankSum
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SIO_000300: -1.92e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
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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: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.599653379549393e-4
allele num: 11540
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

African
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allele count: 11
allele frequency: 1.05708245243129e-3
allele num: 10406
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -5.292e0

MQ
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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DP
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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SIO_000300: -2.57e-1

QD
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ClippingRankSum
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SIO_000300: -1.92e-1

GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66718
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East Asian
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allele frequency: 1.156871818602499e-4
allele num: 8644
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele num: 6612
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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FS
type: SiteQuality
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DP
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ReadPosRankSum
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VQSLOD
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MQ
type: SiteQuality
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

East Asian
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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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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.997601918465228e-5
allele num: 66720
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Other
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South Asian
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ReadPosRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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QD
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VQSLOD
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DP
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MQ
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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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

Latino
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Other
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
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East Asian
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European (Finnish)
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ReadPosRankSum
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ClippingRankSum
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DP
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BaseQRankSum
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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MQ
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FS
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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Other
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num of homozygotes: 0

European (Finnish)
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African
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Latino
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allele frequency: 8.665511265164645e-5
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East Asian
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European (Non-Finnish)
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South Asian
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ReadPosRankSum
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InbreedingCoeff
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FS
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DP
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MQ
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ClippingRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
all individuals: 998
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 50476
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1441
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.514123e6

FS
type: SiteQuality
SIO_000300: 7.61e0

MQRankSum
type: SiteQuality
SIO_000300: 1.15e0

QD
type: SiteQuality
SIO_000300: 1.532e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.088e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

GenotypeQuality
all individuals: 1146
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 987
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50480
bin: 9.75e1
variant carriers: 16

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495863805299125e-5
allele num: 66728
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.040943789035392e-3
allele num: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.55e0

FS
type: SiteQuality
SIO_000300: 5.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.383e1

MQ
type: SiteQuality
SIO_000300: 5.955e1

DP
type: SiteQuality
SIO_000300: 3.515153e6

GenotypeQuality
all individuals: 988
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4171
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 737
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GenotypeQuality
all individuals: 1447
bin: 6.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.44e-1

QD
type: SiteQuality
SIO_000300: 1.278e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

DP
type: SiteQuality
SIO_000300: 3.514183e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

FS
type: SiteQuality
SIO_000300: 4.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.669e0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

GenotypeQuality
all individuals: 2
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11
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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
all individuals: 50478
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variant carriers: 1

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

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

GenotypeQuality
all individuals: 1146
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.275e1

MQ
type: SiteQuality
SIO_000300: 5.93e1

VQSLOD
type: SiteQuality
SIO_000300: 7.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 9.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.865e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.57e-1

DP
type: SiteQuality
SIO_000300: 3.514338e6

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

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

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

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 4167
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

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

GenotypeQuality
all individuals: 1453
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variant carriers: 0

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

GenotypeQuality
all individuals: 1000
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 9.25e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.049e0

VQSLOD
type: SiteQuality
SIO_000300: -7.065e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: -1.888e0

QD
type: SiteQuality
SIO_000300: 1.092e1

FS
type: SiteQuality
SIO_000300: 3.139e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

DP
type: SiteQuality
SIO_000300: 3.514241e6

GenotypeQuality
all individuals: 14
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 988
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1453
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.843936190659235e-4
allele num: 10406
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
SIO_000300: 3.529361e6

QD
type: SiteQuality
SIO_000300: 1.296e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.63e-1

GenotypeQuality
all individuals: 999
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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
all individuals: 50486
bin: 9.75e1
variant carriers: 133

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 14
allele frequency: 2.11672210462655e-3
allele num: 6614
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.469010175763182e-4
allele num: 8648
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.726888333653661e-4
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 103
allele frequency: 1.543394869335891e-3
allele num: 66736
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.529361e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.14e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

QD
type: SiteQuality
SIO_000300: 1.296e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.63e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

GenotypeQuality
all individuals: 50482
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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
all individuals: 1146
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.425e0

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.518997e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 50484
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variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
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: 908
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.033e1

MQRankSum
type: SiteQuality
SIO_000300: -1.023e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.084e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.100000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.584e0

VQSLOD
type: SiteQuality
SIO_000300: -1.157e0

DP
type: SiteQuality
SIO_000300: 3.519148e6

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 998
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50486
bin: 9.75e1
variant carriers: 15

GenotypeQuality
all individuals: 987
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1145
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.040703052728955e-3
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 5.765904285988853e-4
allele num: 10406
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.66e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.521161e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.69e-1

MQ
type: SiteQuality
SIO_000300: 5.944e1

VQSLOD
type: SiteQuality
SIO_000300: 5.46e0

QD
type: SiteQuality
SIO_000300: 1.222e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.934e0

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

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

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

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4166
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 996
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1453
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.958e1

FS
type: SiteQuality
SIO_000300: 4.755e0

DP
type: SiteQuality
SIO_000300: 3.519746e6

QD
type: SiteQuality
SIO_000300: 1.271e1

VQSLOD
type: SiteQuality
SIO_000300: 8.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

MQRankSum
type: SiteQuality
SIO_000300: -1.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.1e-2

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1450
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 50483
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 695
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 997
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 734
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 986
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.966e1

QD
type: SiteQuality
SIO_000300: 1.302e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 3.884e0

DP
type: SiteQuality
SIO_000300: 3.519456e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.63e0

VQSLOD
type: SiteQuality
SIO_000300: 9.01e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.25e-1

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

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

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

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 985
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 996
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4129
bin: 6.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1145
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.992805755395684e-5
allele num: 66720
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.34e-1

QD
type: SiteQuality
SIO_000300: 1.145e1

FS
type: SiteQuality
SIO_000300: 1.971e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.947e0

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

MQRankSum
type: SiteQuality
SIO_000300: -3.67e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 3.519958e6

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

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

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

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

GenotypeQuality
all individuals: 1403
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50738
bin: 9.75e1
variant carriers: 724

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

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

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

GenotypeQuality
all individuals: 1130
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 667
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 969
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 31
allele frequency: 2.682589131187262e-3
allele num: 11556
num of homozygotes: 1

African
type: Population
allele count: 4
allele frequency: 3.843936190659235e-4
allele num: 10406
num of homozygotes: 0

Other
type: Population
allele count: 15
allele frequency: 1.651982378854626e-2
allele num: 908
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 341
allele frequency: 5.110911270983213e-3
allele num: 66720
num of homozygotes: 1

South Asian
type: Population
allele count: 341
allele frequency: 2.065414900060569e-2
allele num: 16510
num of homozygotes: 6

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.687e0

MQRankSum
type: SiteQuality
SIO_000300: 2.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.35e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.73e0

FS
type: SiteQuality
SIO_000300: 6.0e-1

DP
type: SiteQuality
SIO_000300: 3.577433e6

QD
type: SiteQuality
SIO_000300: 1.264e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-1

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 728
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1148
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4131
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1446
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50511
bin: 9.75e1
variant carriers: 1

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.534299e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.66e-1

QD
type: SiteQuality
SIO_000300: 1.263e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.44e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.19e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

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

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

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

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

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

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1443
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 678
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 972
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1148
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.66e0

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

FS
type: SiteQuality
SIO_000300: 2.795e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 3.534171e6

QD
type: SiteQuality
SIO_000300: 1.244e1

GenotypeQuality
all individuals: 1149
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 971
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50510
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 676
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4017
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.92e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.869e-1

DP
type: SiteQuality
SIO_000300: 3.533196e6

MQRankSum
type: SiteQuality
SIO_000300: -4.562e0

MQ
type: SiteQuality
SIO_000300: 4.95e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

QD
type: SiteQuality
SIO_000300: 3.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.291e0

GenotypeQuality
all individuals: 677
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3986
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 985
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 973
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variant carriers: 0

GenotypeQuality
all individuals: 50509
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variant carriers: 7

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1424
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 7
allele frequency: 8.094357076780758e-4
allele num: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.539e0

DP
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SIO_000300: 3.533208e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
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SIO_000300: 7.93e-1

FS
type: SiteQuality
SIO_000300: 2.456e0

QD
type: SiteQuality
SIO_000300: 1.255e1

ClippingRankSum
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SIO_000300: -3.93e-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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bin: 5.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 7.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.794e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 1.18e0

QD
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SIO_000300: 1.298e1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.149e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.84e-1

FS
type: SiteQuality
SIO_000300: 4.727e0

VQSLOD
type: SiteQuality
SIO_000300: 3.08e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

QD
type: SiteQuality
SIO_000300: 1.495e1

DP
type: SiteQuality
SIO_000300: 3.527307e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.88e-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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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.03e-1

MQ
type: SiteQuality
SIO_000300: 5.906e1

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

DP
type: SiteQuality
SIO_000300: 3.526309e6

QD
type: SiteQuality
SIO_000300: 1.152e1

VQSLOD
type: SiteQuality
SIO_000300: 7.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

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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variant carriers: 15

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 6.036217303822937e-4
allele num: 9940
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.355544175678525e-4
allele num: 66394
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16340
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.91e0

QD
type: SiteQuality
SIO_000300: 1.665e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 2.89778e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.92e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.18e0

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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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9966
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

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

European (Finnish)
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allele count: 6
allele frequency: 9.104704097116844e-4
allele num: 6590
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66432
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-1

DP
type: SiteQuality
SIO_000300: 2.903865e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

VQSLOD
type: SiteQuality
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ClippingRankSum
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SIO_000300: 9.25e-1

FS
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
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SIO_000300: 1.3e1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504981488727689e-5
allele num: 66446
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Other
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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DP
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FS
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MQ
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10132
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66510
num of homozygotes: 0

Latino
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allele frequency: 1.73190162798753e-4
allele num: 11548
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.26e-1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
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DP
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GenotypeQuality
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variant carriers: 18

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

Other
type: Population
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African
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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East Asian
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allele count: 18
allele frequency: 2.084781097984711e-3
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66570
num of homozygotes: 0

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
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BaseQRankSum
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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variant carriers: 2

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.315886984715146e-4
allele num: 8636
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66594
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Other
type: Population
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6602
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

BaseQRankSum
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SIO_000300: 4.94e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.69e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.02e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.922966e6

VQSLOD
type: SiteQuality
SIO_000300: 9.350000000000001e-1

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

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2631
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6170
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2570
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2987
bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.501935832407936e-5
allele num: 66638
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.976e0

DP
type: SiteQuality
SIO_000300: 2.927484e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.56e-1

QD
type: SiteQuality
SIO_000300: 1.219e1

GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 90
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40088
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2987
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 8.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.976e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.56e-1

DP
type: SiteQuality
SIO_000300: 2.927484e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.5e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

QD
type: SiteQuality
SIO_000300: 1.219e1

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

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

GenotypeQuality
all individuals: 23
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2987
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40088
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 1640
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6170
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2570
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 1.800774332963174e-4
allele num: 66638
num of homozygotes: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.56e-1

DP
type: SiteQuality
SIO_000300: 2.927484e6

QD
type: SiteQuality
SIO_000300: 1.219e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.976e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-1

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

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

GenotypeQuality
all individuals: 2571
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2987
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 85
allele frequency: 9.831135785334259e-3
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 23
allele frequency: 1.394446465381351e-3
allele num: 16494
num of homozygotes: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.31e-2

DP
type: SiteQuality
SIO_000300: 2.933113e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.257e1

GenotypeQuality
all individuals: 2855
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2633
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1555
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 40079
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2993
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2577
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6215
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66648
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.92e-2

DP
type: SiteQuality
SIO_000300: 2.927087e6

VQSLOD
type: SiteQuality
SIO_000300: -2.751e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.763e0

MQRankSum
type: SiteQuality
SIO_000300: -1.401e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.51e0

QD
type: SiteQuality
SIO_000300: 1.282e1

FS
type: SiteQuality
SIO_000300: 7.85e-1

GenotypeQuality
all individuals: 2992
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40105
bin: 9.75e1
variant carriers: 49

GenotypeQuality
all individuals: 1555
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2571
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6210
bin: 6.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 49
allele frequency: 2.96969696969697e-3
allele num: 16500
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66650
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.62e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.315e0

MQRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.426e0

QD
type: SiteQuality
SIO_000300: 1.132e1

VQSLOD
type: SiteQuality
SIO_000300: -4.895e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.72e0

DP
type: SiteQuality
SIO_000300: 2.929234e6

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

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 1639
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 2570
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 1559
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variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40089
bin: 9.75e1
variant carriers: 18

South Asian
type: Population
allele count: 17
allele frequency: 1.030178160223003e-3
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.967e1

FS
type: SiteQuality
SIO_000300: 3.864e0

QD
type: SiteQuality
SIO_000300: 1.225e1

MQRankSum
type: SiteQuality
SIO_000300: -3.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.98e-1

DP
type: SiteQuality
SIO_000300: 2.928728e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.571e0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 2574
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variant carriers: 0

GenotypeQuality
all individuals: 6230
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 63
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 2864
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 40076
bin: 9.75e1
variant carriers: 22

GenotypeQuality
all individuals: 1638
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2641
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 19
allele frequency: 1.644736842105263e-3
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999940001199976e-5
allele num: 66668
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.929735e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.53e-2

MQ
type: SiteQuality
SIO_000300: 5.947e1

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.205e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

VQSLOD
type: SiteQuality
SIO_000300: 3.15e0

GenotypeQuality
all individuals: 2863
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 54
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variant carriers: 0

GenotypeQuality
all individuals: 6260
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1561
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 1639
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GenotypeQuality
all individuals: 2998
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variant carriers: 0

GenotypeQuality
all individuals: 2575
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

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

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.731601731601732e-4
allele num: 11550
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.928362e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.66e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.89e0

QD
type: SiteQuality
SIO_000300: 1.343e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

VQSLOD
type: SiteQuality
SIO_000300: -2.259e-1

FS
type: SiteQuality
SIO_000300: 4.294e0

MQ
type: SiteQuality
SIO_000300: 5.918e1

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

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

GenotypeQuality
all individuals: 2998
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
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GenotypeQuality
all individuals: 2859
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40078
bin: 9.75e1
variant carriers: 10

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2641
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2573
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 10
allele frequency: 9.611687812379854e-4
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.99e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.776e0

QD
type: SiteQuality
SIO_000300: 1.127e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

FS
type: SiteQuality
SIO_000300: 5.92e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

DP
type: SiteQuality
SIO_000300: 2.928945e6

VQSLOD
type: SiteQuality
SIO_000300: 3.76e0

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

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

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2862
bin: 6.75e1
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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variant carriers: 60

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 6264
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.059642749016046e-3
allele num: 6606
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 51
allele frequency: 7.646176911544227e-4
allele num: 66700
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.933599e6

FS
type: SiteQuality
SIO_000300: 5.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 3.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e0

QD
type: SiteQuality
SIO_000300: 1.354e1

GenotypeQuality
all individuals: 6259
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 7
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variant carriers: 0

GenotypeQuality
all individuals: 2569
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 8.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.497751124437781e-5
allele num: 66700
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 8.179999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.13e-1

FS
type: SiteQuality
SIO_000300: 4.095e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.32e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.958e1

DP
type: SiteQuality
SIO_000300: 2.929922e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.49e-1

QD
type: SiteQuality
SIO_000300: 1.511e1

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

GenotypeQuality
all individuals: 39
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1639
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.996641880546894e-5
allele num: 66704
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.108e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

VQSLOD
type: SiteQuality
SIO_000300: 2.08e0

DP
type: SiteQuality
SIO_000300: 2.930253e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.63e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.57e-1

QD
type: SiteQuality
SIO_000300: 1.274e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

MQRankSum
type: SiteQuality
SIO_000300: -1.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.004e0

GenotypeQuality
all individuals: 2571
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2644
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2997
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.27e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.62e0

FS
type: SiteQuality
SIO_000300: 1.051e0

MQRankSum
type: SiteQuality
SIO_000300: 4.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.69e-1

QD
type: SiteQuality
SIO_000300: 1.262e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.89e-1

DP
type: SiteQuality
SIO_000300: 2.930005e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-2

MQ
type: SiteQuality
SIO_000300: 5.946e1

GenotypeQuality
all individuals: 40085
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2863
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1638
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2645
bin: 8.25e1
variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.08e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.03e0

VQSLOD
type: SiteQuality
SIO_000300: -8.39e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.114e1

MQRankSum
type: SiteQuality
SIO_000300: 8.42e-1

DP
type: SiteQuality
SIO_000300: 2.929939e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.83e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 46

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.731601731601732e-4
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 40
allele frequency: 5.995563283170454e-4
allele num: 66716
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.82e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.623e0

DP
type: SiteQuality
SIO_000300: 2.933077e6

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

FS
type: SiteQuality
SIO_000300: 5.23e-1

QD
type: SiteQuality
SIO_000300: 1.15e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.08e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

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: 908
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
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MQ
type: SiteQuality
SIO_000300: 5.829e1

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.9e-2

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

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

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

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

East Asian
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allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 908
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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DP
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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FS
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SIO_000300: 1.381e0

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
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SIO_000300: 5.869e1

BaseQRankSum
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SIO_000300: -2.121e0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66724
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
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Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 3.633720930232558e-4
allele num: 16512
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
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Latino
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: -9.69e-1

ReadPosRankSum
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MQ
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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QD
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DP
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FS
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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Other
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
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

DP
type: SiteQuality
SIO_000300: 2.929897e6

MQRankSum
type: SiteQuality
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QD
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FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.811e1

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.929875e6

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
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VQSLOD
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QD
type: SiteQuality
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MQ
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BaseQRankSum
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

African
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allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
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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num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 6.056201550387597e-5
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ClippingRankSum
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FS
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DP
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MQRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

African
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Latino
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Other
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South Asian
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European (Non-Finnish)
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num of homozygotes: 0

East Asian
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MQ
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FS
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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MQRankSum
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QD
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BaseQRankSum
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DP
type: SiteQuality
SIO_000300: 2.929522e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.179e0