14-93678369-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678369
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678369
    reference: chr 14
allele count: 3
allele frequency: 4.015849218248019e-5
allele num: 74704
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*47-9A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.317-9A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.118-9A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.255-9A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1315A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.123-9A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.346-9A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl protein: ENSP00000451369
  ensembl transcript: ENST00000557574
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557574.1:c.403-9A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2906A>G
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1726
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21737
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

14-93678386-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678386
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678386
    reference: chr 14
allele count: 3
allele frequency: 3.179245882876582e-5
allele num: 94362
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.354A>G
  hgvsp: ENST00000013070.6:c.354A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.263A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1332A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.131A>G
  hgvsp: ENST00000553857.1:c.131A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.325A>G
  hgvsp: ENST00000555113.1:c.325A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*55A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.126A>G
  hgvsp: ENST00000416753.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2889A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000259066
  ensembl protein: ENSP00000451369
  ensembl transcript: ENST00000557574
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557574.1:c.411A>G
  hgvsp: ENST00000557574.1:c.411A>G(p.%3D)
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31602
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32614
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala137Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

14-93678389-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678389
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678389
    reference: chr 14
allele count: 1
allele frequency: 1.039047401342449e-5
allele num: 96242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.129G>A
  hgvsp: ENST00000416753.1:c.129G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*58G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.357G>A
  hgvsp: ENST00000013070.6:c.357G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.266G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.134G>A
  hgvsp: ENST00000553857.1:c.134G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000259066
  ensembl protein: ENSP00000451369
  ensembl transcript: ENST00000557574
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557574.1:c.414G>A
  hgvsp: ENST00000557574.1:c.414G>A(p.%3D)
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1335G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.328G>A
  hgvsp: ENST00000555113.1:c.328G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2886G>A
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32349
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12559
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1702
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys138Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS

14-93678399-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678399
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678399
    reference: chr 14
allele count: 1
allele frequency: 9.853770052422056e-6
allele num: 101484
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.139G>C
  hgvsp: ENSP00000391706.1:p.Gly47Arg
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.144G>C
  hgvsp: ENSP00000451785.1:p.Gly49Arg
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2876G>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.367G>C
  hgvsp: ENSP00000013070.6:p.Gly123Arg
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.276G>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000259066
  ensembl protein: ENSP00000451369
  ensembl transcript: ENST00000557574
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557574.1:c.424G>C
  hgvsp: ENSP00000451369.1:p.Gly142Arg
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*68G>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.338G>C
  hgvsp: ENSP00000451051.1:p.Gly114Arg
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1345G>C
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9766
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly142Arg
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

14-93678401-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678401
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678401
    reference: chr 14
allele count: 1
allele frequency: 9.776700168159243e-6
allele num: 102284
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000259066
  ensembl protein: ENSP00000451369
  ensembl transcript: ENST00000557574
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557574.1:c.426C>T
  hgvsp: ENST00000557574.1:c.426C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.340C>T
  hgvsp: ENST00000555113.1:c.340C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.278C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.141C>T
  hgvsp: ENST00000416753.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.369C>T
  hgvsp: ENST00000013070.6:c.369C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1347C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.146C>T
  hgvsp: ENST00000553857.1:c.146C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*70C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2874C>T
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34721
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9794
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 447
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6977
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly142Gly
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

14-93678416-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678416
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678416
    reference: chr 14
allele count: 1
allele frequency: 9.431648840850358e-6
allele num: 106026
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.384C>T
  hgvsp: ENST00000013070.6:c.384C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000259066
  ensembl protein: ENSP00000451369
  ensembl transcript: ENST00000557574
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557574.1:c.441C>T
  hgvsp: ENST00000557574.1:c.441C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.355C>T
  hgvsp: ENST00000555113.1:c.355C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.161C>T
  hgvsp: ENST00000553857.1:c.161C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.156C>T
  hgvsp: ENST00000416753.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.293C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*85C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1362C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2859C>T
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7559
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1970
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp147Asp
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

14-93678419-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678419
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678419
    reference: chr 14
allele count: 2
allele frequency: 1.885831746091614e-5
allele num: 106054
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2856C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000259066
  ensembl protein: ENSP00000451369
  ensembl transcript: ENST00000557574
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557574.1:c.444C>T
  hgvsp: ENST00000557574.1:c.444C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*88C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.164C>T
  hgvsp: ENST00000553857.1:c.164C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.296C>T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.387C>T
  hgvsp: ENST00000013070.6:c.387C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.159C>T
  hgvsp: ENST00000416753.1:c.159C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.358C>T
  hgvsp: ENST00000555113.1:c.358C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1365C>T
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5885
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8427
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 401
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asn148Asn
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

14-93678431-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678431
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678431
    reference: chr 14
allele count: 1
allele frequency: 9.458590291702925e-6
allele num: 105724
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.399G>A
  hgvsp: ENST00000013070.6:c.399G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.308G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.176G>A
  hgvsp: ENST00000553857.1:c.176G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.171G>A
  hgvsp: ENST00000416753.1:c.171G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2844G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1377G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*100G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000259066
  ensembl protein: ENSP00000451369
  ensembl transcript: ENST00000557574
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557574.1:c.456G>A
  hgvsp: ENST00000557574.1:c.456G>A(p.%3D)
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.370G>A
  hgvsp: ENST00000555113.1:c.370G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9359
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu152Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

14-93678448-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678448
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678448
    reference: chr 14
allele count: 1
allele frequency: 9.844457570387871e-6
allele num: 101580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.325G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.193G>A
  hgvsp: ENSP00000451785.1:p.Arg65Lys
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000259066
  ensembl protein: ENSP00000451369
  ensembl transcript: ENST00000557574
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557574.1:c.473G>A
  hgvsp: ENSP00000451369.1:p.Arg158Lys
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.387G>A
  hgvsp: ENSP00000451051.1:p.Arg130Lys
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.188G>A
  hgvsp: ENSP00000391706.1:p.Arg63Lys
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*117G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1394G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.416G>A
  hgvsp: ENSP00000013070.6:p.Arg139Lys
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2827G>A
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29431
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5942
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 958
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9653
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg158Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-93678465-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678465
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678466
    reference: chr 14
allele count: 1
allele frequency: 1.060715346429632e-5
allele num: 94276
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.212dupA
  hgvsp: ENSP00000451785.1:p.Asp72ArgfsTer6
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2808dupA
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1413dupA
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.435dupA
  hgvsp: ENSP00000013070.6:p.Asp146ArgfsTer6
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.406dupA
  hgvsp: ENSP00000451051.1:p.Asp137ArgfsTer6
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000259066
  ensembl protein: ENSP00000451369
  ensembl transcript: ENST00000557574
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557574.1:c.492dupA
  hgvsp: ENSP00000451369.1:p.Asp165ArgfsTer?
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.344dupA
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*136dupA
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.207dupA
  hgvsp: ENSP00000391706.1:p.Asp70ArgfsTer6
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12821
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21235
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10446
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 692
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1513
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 376
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp165ArgfsTer?
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

14-93678470-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678470
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678470
    reference: chr 14
allele count: 4
allele frequency: 4.355969856688592e-5
allele num: 91828
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2805C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.210C>T
  hgvsp: ENST00000416753.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.215C>T
  hgvsp: ENST00000553857.1:c.215C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000259066
  ensembl protein: ENSP00000451369
  ensembl transcript: ENST00000557574
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557574.1:c.495C>T
  hgvsp: ENST00000557574.1:c.495C>T(p.%3D)
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1416C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*139C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.347C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.409C>T
  hgvsp: ENST00000555113.1:c.409C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.438C>T
  hgvsp: ENST00000013070.6:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5006
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12084
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13697
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp165Asp
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

14-93678471-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678471
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678471
    reference: chr 14
allele count: 1
allele frequency: 1.101661305248315e-5
allele num: 90772
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.410G>A
  hgvsp: ENSP00000451051.1:p.Glu138Lys
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.348G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.211G>A
  hgvsp: ENSP00000391706.1:p.Glu71Lys
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.439G>A
  hgvsp: ENSP00000013070.6:p.Glu147Lys
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*140G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000259066
  ensembl protein: ENSP00000451369
  ensembl transcript: ENST00000557574
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557574.1:c.496G>A
  hgvsp: ENSP00000451369.1:p.Glu166Lys
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1417G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.216G>A
  hgvsp: ENSP00000451785.1:p.Glu73Lys
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2804G>A
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14081
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12840
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17697
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1016
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu166Lys
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

14-93678480-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678480
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678480
    reference: chr 14
allele count: 4
allele frequency: 4.631988512668489e-5
allele num: 86356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2795G>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*142+7G>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.441+7G>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.350+7G>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.412+7G>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.218+7G>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.213+7G>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1426G>T
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15667
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13064
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6979
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2703
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1705
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
hgvs: c.441+7G>T
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/14-93678488-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678488
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678488
    reference: chr 14
allele count: 1
allele frequency: 1.224379851605162e-5
allele num: 81674
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.350+15A>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.213+15A>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.412+15A>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1434A>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2787A>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*142+15A>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.441+15A>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.218+15A>C
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16812
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19367
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 807
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3268
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 758
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6976
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

14-93678490-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678490
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678490
    reference: chr 14
allele count: 1
allele frequency: 1.24480294769338e-5
allele num: 80334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2785T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.218+17T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1436T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.350+17T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.441+17T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.412+17T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.213+17T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*142+17T>C
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19755
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17059
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8071
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3380
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3455
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

14-93678494-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678494
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678494
    reference: chr 14
allele count: 27
allele frequency: 3.492975238686641e-4
allele num: 77298
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*142+21A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.218+21A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2781A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.350+21A>G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.441+21A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.213+21A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.412+21A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1440A>G
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3080
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 17541
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20289
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5312
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1364
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1610
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

14-93678501-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678501
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678501
    reference: chr 14
allele count: 2
allele frequency: 2.748083211959658e-5
allele num: 72778
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.218+28G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.350+28G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*142+28G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1447G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.441+28G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.213+28G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.412+28G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2774G>A
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3144
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19861
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1805
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1770
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1561
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2110
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5769
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/14-93678508-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678508
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678508
    reference: chr 14
allele count: 4
allele frequency: 6.115646882549002e-5
allele num: 65406
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.441+35C>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2767C>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.412+35C>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*142+35C>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.218+35C>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.350+35C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.213+35C>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1454C>A
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6728
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2345
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20294
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17587
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21622
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7763
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3669
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

14-93678511-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678511
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678511
    reference: chr 14
allele count: 1
allele frequency: 1.592255270364945e-5
allele num: 62804
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2764C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.350+38C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.412+38C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.213+38C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.218+38C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1457C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*142+38C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.441+38C>G
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7006
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3633
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6977
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8125
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20380
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4219
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 779
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

14-93678522-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93678522
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93678522
    reference: chr 14
allele count: 586
allele frequency: 1.040372119447502e-2
allele num: 56326
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.345+1468A>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-2753A>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.412+49A>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.218+49A>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.441+49A>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.350+49A>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.213+49A>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*142+49A>T
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 4.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 2.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 7227
  bin: 2.5e0
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 24456
  bin: 7.5e0
  variant carriers: 368
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13492
  bin: 1.25e1
  variant carriers: 289
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 2.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 9.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 6.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3332
  bin: 1.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 8186
  bin: 7.5e0
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 8.75e1
  variant carriers: 56
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16096
  bin: 2.25e1
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 1853
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 8.25e1
  variant carriers: 38
genotype quality: GenotypeQuality
  all individuals: 5198
  bin: 1.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 4.25e1
  variant carriers: 13
num of homozygotes: 4
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

14-93681225-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681225
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681225
    reference: chr 14
allele count: 1
allele frequency: 8.794610662585968e-6
allele num: 113706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.351-50C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.413-50C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*143-50C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-50C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.214-50C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.346-50C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.219-50C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.442-50C>T
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12689
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12743
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2871
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1900
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17341
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3668
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9078
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3693
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 771
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-93681227-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681227
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681227
    reference: chr 14
allele count: 1
allele frequency: 8.774546794658055e-6
allele num: 113966
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.346-48T>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-48T>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*143-48T>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.214-48T>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.219-48T>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.442-48T>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.413-48T>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.351-48T>G
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8762
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13580
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11865
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2868
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9486
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 329
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4544
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18763
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 556
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD

14-93681234-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681234
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681234
    reference: chr 14
allele count: 1
allele frequency: 8.793837278834993e-6
allele num: 113716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.413-41G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.442-41G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.346-41G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.219-41G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.351-41G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*143-41G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-41G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.214-41G>A
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6931
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1079
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8946
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4070
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9069
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25328
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3486
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4163
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

14-93681240-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681240
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681240
    reference: chr 14
allele count: 2
allele frequency: 1.750485759798344e-5
allele num: 114254
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.442-35A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.413-35A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*143-35A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-35A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.219-35A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.351-35A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.346-35A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.214-35A>G
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22025
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9746
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2964
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7782
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3385
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9069
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3187
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1618
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

14-93681241-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681241
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681241
    reference: chr 14
allele count: 10
allele frequency: 8.751050126015122e-5
allele num: 114272
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.442-34A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.351-34A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.219-34A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.413-34A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-34A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*143-34A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.346-34A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.214-34A>G
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9817
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22473
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2983
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7576
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3382
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4062
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3064
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1596
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1459
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

14-93681242-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681242
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681242
    reference: chr 14
allele count: 1
allele frequency: 8.747528823107472e-6
allele num: 114318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.413-33T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.442-33T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.346-33T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-33T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.219-33T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*143-33T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.214-33T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.351-33T>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9856
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2989
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30524
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1227
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4062
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1578
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-93681248-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681248
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681248
    reference: chr 14
allele count: 1
allele frequency: 8.734539864439941e-6
allele num: 114488
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.214-27C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-27C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.219-27C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.442-27C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.413-27C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.346-27C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.351-27C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*143-27C>T
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3992
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1433
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 907
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9065
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

14-93681266-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681266
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681266
    reference: chr 14
allele count: 1
allele frequency: 8.645881966419394e-6
allele num: 115662
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.351-9C>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*143-9C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.219-9C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.442-9C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.151-9C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.413-9C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.214-9C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.346-9C>G
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2811
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 935
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37857
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1109
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-93681299-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681299
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681299
    reference: chr 14
allele count: 17
allele frequency: 1.460757187784633e-4
allele num: 116378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.238G>A
  hgvsp: ENSP00000391706.1:p.Val80Ile
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*167G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.243G>A
  hgvsp: ENSP00000451785.1:p.Val82Ile
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.466G>A
  hgvsp: ENSP00000013070.6:p.Val156Ile
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.375G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.175G>A
  hgvsp: ENSP00000451022.1:p.Val59Ile
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.437G>A
  hgvsp: ENSP00000451051.1:p.Val147Ile
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.370G>A
  hgvsp: ENSP00000450645.1:p.Val124Ile
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3294
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29137
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39698
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9075
  bin: 9.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val156Ile
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

14-93681301-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681301
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681301
    reference: chr 14
allele count: 1
allele frequency: 8.601114704465699e-6
allele num: 116264
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*169A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.177A>G
  hgvsp: ENST00000556871.1:c.177A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.439A>G
  hgvsp: ENST00000555113.1:c.439A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.377A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.240A>G
  hgvsp: ENST00000416753.1:c.240A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.468A>G
  hgvsp: ENST00000013070.6:c.468A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.372A>G
  hgvsp: ENST00000554232.1:c.372A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.245A>G
  hgvsp: ENST00000553857.1:c.245A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39286
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3599
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val156Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

14-93681317-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681317
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681317
    reference: chr 14
allele count: 1
allele frequency: 8.692175303791527e-6
allele num: 115046
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.193T>C
  hgvsp: ENSP00000451022.1:p.Phe65Leu
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.256T>C
  hgvsp: ENSP00000391706.1:p.Phe86Leu
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.455T>C
  hgvsp: ENSP00000451051.1:p.Phe153Leu
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.261T>C
  hgvsp: ENSP00000451785.1:p.Phe88Leu
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.388T>C
  hgvsp: ENSP00000450645.1:p.Phe130Leu
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.393T>C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.484T>C
  hgvsp: ENSP00000013070.6:p.Phe162Leu
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*185T>C
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3223
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9064
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 717
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4994
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3532
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Phe162Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP

14-93681330-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681330
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681330
    reference: chr 14
allele count: 1
allele frequency: 8.859907148173087e-6
allele num: 112868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.204+2T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.466+2T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.404+2T>C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.399+2T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.495+2T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.267+2T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*196+2T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.272+2T>C
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3174
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12593
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34792
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9061
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 252
  bin: 8.75e1
  variant carriers: 0
hgvs: c.495+2T>C
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS

14-93681354-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681354
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681354
    reference: chr 14
allele count: 27
allele frequency: 2.530791294077948e-4
allele num: 106686
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.399+26A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.495+26A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.404+26A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*196+26A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.466+26A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.267+26A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.272+26A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.204+26A>G
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10074
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2777
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3462
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8696
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17985
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 716
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18493
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19491
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9073
  bin: 9.75e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

14-93681356-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681356
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681356
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 105714
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.495+28C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*196+28C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.267+28C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.404+28C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.399+28C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.204+28C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.466+28C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.272+28C>T
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3939
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15099
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20700
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 7.75e1
  variant carriers: 0
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: C
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

14-93681359-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681359
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681359
    reference: chr 14
allele count: 1
allele frequency: 9.514023670890893e-6
allele num: 105108
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.204+31T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.495+31T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*196+31T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.466+31T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.399+31T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.267+31T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.404+31T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.272+31T>C
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6962
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9052
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

14-93681368-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681368
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681368
    reference: chr 14
allele count: 1
allele frequency: 1.01055014349812e-5
allele num: 98956
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.399+40C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.272+40C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.204+40C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.404+40C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.267+40C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*196+40C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.466+40C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.495+40C>G
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10757
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5141
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5114
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2795
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20529
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

14-93681375-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681375
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681375
    reference: chr 14
allele count: 1
allele frequency: 1.140068860159154e-5
allele num: 87714
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.466+47A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.267+47A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.399+47A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.495+47A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.204+47A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.404+47A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.272+47A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*196+47A>G
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10536
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3216
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1935
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1617
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14013
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9050
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3747
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

14-93681376-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681376
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681375
    reference: chr 14
allele count: 1
allele frequency: 1.14035487843817e-5
allele num: 87692
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.404+51delA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.267+51delA
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.204+51delA
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*196+51delA
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.495+51delA
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.272+51delA
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.466+51delA
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.399+51delA
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10511
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4998
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4500
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6827
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5364
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 831
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: TA
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

14-93681506-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681506
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681505
    reference: chr 14
allele count: 3
allele frequency: 1.26528890763391e-4
allele num: 23710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.268-15delG
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*197-15delG
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.496-15delG
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.205-15delG
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.405-15delG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.467-15delG
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.400-15delG
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.273-15delG
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26582
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4336
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20624
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3057
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24202
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16234
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: TG
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ

14-93681507-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681507
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681507
    reference: chr 14
allele count: 13
allele frequency: 5.436146190516015e-4
allele num: 23914
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.273-15G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.400-15G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.496-15G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*197-15G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.268-15G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.405-15G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.467-15G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.205-15G>A
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21226
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 26002
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23834
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2135
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2859
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 1
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

14-93681513-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681513
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681513
    reference: chr 14
allele count: 1
allele frequency: 4.040404040404041e-5
allele num: 24750
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.400-9T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.496-9T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.205-9T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.268-9T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.405-9T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.273-9T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.467-9T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*197-9T>C
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21974
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25286
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4341
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22419
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20644
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

14-93681523-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681523
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681523
    reference: chr 14
allele count: 1
allele frequency: 3.699319325244155e-5
allele num: 27032
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.497A>G
  hgvsp: ENSP00000013070.6:p.His166Arg
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.406A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.274A>G
  hgvsp: ENSP00000451785.1:p.His92Arg
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.269A>G
  hgvsp: ENSP00000391706.1:p.His90Arg
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.401A>G
  hgvsp: ENSP00000450645.1:p.His134Arg
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.206A>G
  hgvsp: ENSP00000451022.1:p.His69Arg
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*198A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.468A>G
  hgvsp: ENSP00000451051.1:p.His157Arg
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15934
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1254
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9381
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28282
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His166Arg
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS

14-93681529-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681529
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681529
    reference: chr 14
allele count: 2
allele frequency: 7.09622480840193e-5
allele num: 28184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.275G>A
  hgvsp: ENSP00000391706.1:p.Gly92Asp
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.212G>A
  hgvsp: ENSP00000451022.1:p.Gly71Asp
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.280G>A
  hgvsp: ENSP00000451785.1:p.Gly94Asp
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.412G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.474G>A
  hgvsp: ENSP00000451051.1:p.Gly159Asp
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*204G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.407G>A
  hgvsp: ENSP00000450645.1:p.Gly136Asp
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.503G>A
  hgvsp: ENSP00000013070.6:p.Gly168Asp
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32246
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13681
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1991
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13188
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly168Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/14-93681540-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681540
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681540
    reference: chr 14
allele count: 1
allele frequency: 3.152386356471849e-5
allele num: 31722
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*215C>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.418C>A
  hgvsp: ENSP00000450645.1:p.Pro140Thr
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.223C>A
  hgvsp: ENSP00000451022.1:p.Pro75Thr
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.514C>A
  hgvsp: ENSP00000013070.6:p.Pro172Thr
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.485C>A
  hgvsp: ENSP00000451051.1:p.Pro163Thr
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.286C>A
  hgvsp: ENSP00000391706.1:p.Pro96Thr
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.291C>A
  hgvsp: ENSP00000451785.1:p.Pro98Thr
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.423C>A
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10321
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33946
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10042
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro172Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

14-93681541-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681541
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681541
    reference: chr 14
allele count: 1
allele frequency: 3.117595710188303e-5
allele num: 32076
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.292C>G
  hgvsp: ENSP00000451785.1:p.Pro98Arg
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.419C>G
  hgvsp: ENSP00000450645.1:p.Pro140Arg
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*216C>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.515C>G
  hgvsp: ENSP00000013070.6:p.Pro172Arg
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.287C>G
  hgvsp: ENSP00000391706.1:p.Pro96Arg
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.486C>G
  hgvsp: ENSP00000451051.1:p.Pro163Arg
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.224C>G
  hgvsp: ENSP00000451022.1:p.Pro75Arg
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.424C>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10092
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34027
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2544
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32080
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro172Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: African
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

14-93681541-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681541
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681540
    reference: chr 14
allele count: 1
allele frequency: 3.117595710188303e-5
allele num: 32076
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.420delT
  hgvsp: ENSP00000450645.1:p.Glu141ArgfsTer14
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.293delT
  hgvsp: ENSP00000451785.1:p.Glu99ArgfsTer14
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.225delT
  hgvsp: ENSP00000451022.1:p.Glu76ArgfsTer14
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.516delT
  hgvsp: ENSP00000013070.6:p.Glu173ArgfsTer14
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.288delT
  hgvsp: ENSP00000391706.1:p.Glu97ArgfsTer14
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.425delT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.487delT
  hgvsp: ENSP00000451051.1:p.Pro164ProfsTer?
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*217delT
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2549
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34027
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10092
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 913
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2029
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9806
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32080
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu173ArgfsTer14
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: CT
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

14-93681545-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681545
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681545
    reference: chr 14
allele count: 1
allele frequency: 2.996703626011388e-5
allele num: 33370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.228G>T
  hgvsp: ENSP00000451022.1:p.Glu76Asp
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.296G>T
  hgvsp: ENSP00000451785.1:p.Glu99Asp
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.291G>T
  hgvsp: ENSP00000391706.1:p.Glu97Asp
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*220G>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.423G>T
  hgvsp: ENSP00000450645.1:p.Glu141Asp
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.428G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451051
  ensembl transcript: ENST00000555113
  gene symbol: UBR7
  hgvsc: ENST00000555113.1:c.490G>T
  hgvsp: ENSP00000451051.1:p.Glu164Asp
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.519G>T
  hgvsp: ENSP00000013070.6:p.Glu173Asp
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34350
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9381
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8944
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 847
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32702
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu173Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

14-93681546-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681546
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681546
    reference: chr 14
allele count: 1
allele frequency: 2.964368293116737e-5
allele num: 33734
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.424A>G
  hgvsp: ENSP00000450645.1:p.Ser142Gly
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.292A>G
  hgvsp: ENSP00000391706.1:p.Ser98Gly
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*221A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.229A>G
  hgvsp: ENSP00000451022.1:p.Ser77Gly
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.520A>G
  hgvsp: ENSP00000013070.6:p.Ser174Gly
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.429A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.297A>G
  hgvsp: ENSP00000451785.1:p.Ser100Gly
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8967
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2783
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 757
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3055
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 852
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1829
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8762
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9382
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ser174Gly
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

14-93681564-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681564
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681564
    reference: chr 14
allele count: 1
allele frequency: 2.621919244887257e-5
allele num: 38140
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.442A>T
  hgvsp: ENSP00000450645.1:p.Met148Leu
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.247A>T
  hgvsp: ENSP00000451022.1:p.Met83Leu
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.310A>T
  hgvsp: ENSP00000391706.1:p.Met104Leu
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.447A>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.315A>T
  hgvsp: ENSP00000451785.1:p.Met106Leu
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*239A>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.538A>T
  hgvsp: ENSP00000013070.6:p.Met180Leu
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7024
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 774
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1656
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33598
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Met180Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS

14-93681576-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681576
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681576
    reference: chr 14
allele count: 1
allele frequency: 2.559639602743934e-5
allele num: 39068
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.259G>A
  hgvsp: ENSP00000451022.1:p.Ala87Thr
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.459G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.322G>A
  hgvsp: ENSP00000391706.1:p.Ala108Thr
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*251G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.327G>A
  hgvsp: ENSP00000451785.1:p.Ala110Thr
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.550G>A
  hgvsp: ENSP00000013070.6:p.Ala184Thr
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.454G>A
  hgvsp: ENSP00000450645.1:p.Ala152Thr
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4014
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33481
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33585
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7307
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala184Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

14-93681581-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681581
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681581
    reference: chr 14
allele count: 1
allele frequency: 2.584112874050338e-5
allele num: 38698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*256C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.264C>T
  hgvsp: ENST00000556871.1:c.264C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.327C>T
  hgvsp: ENST00000416753.1:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.555C>T
  hgvsp: ENST00000013070.6:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.332C>T
  hgvsp: ENST00000553857.1:c.332C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.459C>T
  hgvsp: ENST00000554232.1:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.464C>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32844
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7996
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3607
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32955
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 788
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8084
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9383
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3673
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Cys185Cys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

14-93681589-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681589
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681589
    reference: chr 14
allele count: 5
allele frequency: 1.319679054054054e-4
allele num: 37888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.340G>A
  hgvsp: ENSP00000451785.1:p.Arg114His
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.272G>A
  hgvsp: ENSP00000451022.1:p.Arg91His
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*264G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.467G>A
  hgvsp: ENSP00000450645.1:p.Arg156His
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.335G>A
  hgvsp: ENSP00000391706.1:p.Arg112His
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.563G>A
  hgvsp: ENSP00000013070.6:p.Arg188His
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.472G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2836
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31813
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 1.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9434
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2933
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg188His
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

14-93681605-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681605
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681605
    reference: chr 14
allele count: 1
allele frequency: 2.808357672433161e-5
allele num: 35608
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.488G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.356G>T
  hgvsp: ENSP00000451785.1:p.Trp119Cys
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*280G>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.351G>T
  hgvsp: ENSP00000391706.1:p.Trp117Cys
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.288G>T
  hgvsp: ENSP00000451022.1:p.Trp96Cys
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.579G>T
  hgvsp: ENSP00000013070.6:p.Trp193Cys
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.483G>T
  hgvsp: ENSP00000450645.1:p.Trp161Cys
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13248
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28855
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28781
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13307
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 523
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Trp193Cys
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ

14-93681613-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681613
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681613
    reference: chr 14
allele count: 1
allele frequency: 2.922096896733096e-5
allele num: 34222
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.491C>T
  hgvsp: ENSP00000450645.1:p.Ala164Val
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.296C>T
  hgvsp: ENSP00000451022.1:p.Ala99Val
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*288C>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.359C>T
  hgvsp: ENSP00000391706.1:p.Ala120Val
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.364C>T
  hgvsp: ENSP00000451785.1:p.Ala122Val
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.587C>T
  hgvsp: ENSP00000013070.6:p.Ala196Val
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.496C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15731
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26873
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4345
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1250
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26852
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1362
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 6.75e1
  variant carriers: 1
hgvs: p.Ala196Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-93681617-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681617
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681617
    reference: chr 14
allele count: 1
allele frequency: 3.000300030003e-5
allele num: 33330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.495A>G
  hgvsp: ENST00000554232.1:c.495A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.500A>G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.363A>G
  hgvsp: ENST00000416753.1:c.363A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.300A>G
  hgvsp: ENST00000556871.1:c.300A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.591A>G
  hgvsp: ENST00000013070.6:c.591A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.368A>G
  hgvsp: ENST00000553857.1:c.368A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*292A>G
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5200
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17465
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25514
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 483
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2219
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala197Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

14-93681628-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681628
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681628
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 30536
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.378+1G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*302+1G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.505+1G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.310+1G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.601+1G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.510+1G>A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.373+1G>A
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: splice donor
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21956
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20840
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 1.25e1
  variant carriers: 0
hgvs: c.601+1G>A
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-93681632-GTA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681632
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681630
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 29314
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.310+7_310+8delAT
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.505+7_505+8delAT
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.601+7_601+8delAT
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.510+7_510+8delAT
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.378+7_378+8delAT
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.373+7_373+8delAT
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*302+7_*302+8delAT
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3937
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20190
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18085
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23956
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2394
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1965
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1052
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
hgvs: c.601+7_601+8delAT
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: GTA
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

14-93681644-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681644
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681644
    reference: chr 14
allele count: 1
allele frequency: 3.68758758020503e-5
allele num: 27118
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.601+17A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.378+17A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.510+17A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*302+17A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.505+17A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.373+17A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.310+17A>G
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27922
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16770
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2406
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27297
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9383
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

14-93681645-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681645
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681645
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 26902
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.505+18G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.601+18G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.373+18G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*302+18G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.310+18G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.510+18G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.378+18G>A
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16608
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28086
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13665
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2440
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9382
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

14-93681646-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681646
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681646
    reference: chr 14
allele count: 14
allele frequency: 5.213764337851929e-4
allele num: 26852
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.601+19T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.510+19T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.373+19T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.310+19T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*302+19T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.378+19T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.505+19T>C
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16468
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28245
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27590
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2444
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1828
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

14-93681646-TTGG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681646
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681643
    reference: chr 14
allele count: 1
allele frequency: 3.724117384179949e-5
allele num: 26852
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*302+22_*302+24delGTG
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.373+22_373+24delGTG
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.510+22_510+24delGTG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.378+22_378+24delGTG
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.310+22_310+24delGTG
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.601+22_601+24delGTG
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.505+22_505+24delGTG
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16468
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13596
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2444
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27590
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9387
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: TTGG
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-93681658-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93681658
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93681658
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 25070
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*302+31A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.510+31A>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.310+31A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.601+31A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.505+31A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.378+31A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.373+31A>G
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13583
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30757
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2339
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9384
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3626
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

14-93684824-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93684824
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93684824
    reference: chr 14
allele count: 1
allele frequency: 8.645732466454558e-6
allele num: 115664
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*303-49G>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.311-49G>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.511-49G>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.602-49G>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.506-49G>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.378+3197G>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.374-49G>C
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10900
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6541
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13200
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2306
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3561
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2135
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3069
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18258
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2253
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 905
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1654
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

14-93684833-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93684833
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93684833
    reference: chr 14
allele count: 1
allele frequency: 8.604371020478403e-6
allele num: 116220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.511-40A>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.506-40A>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.374-40A>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.311-40A>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*303-40A>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.378+3206A>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.602-40A>T
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7016
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2070
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2287
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2711
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2172
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3192
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2560
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1054
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

14-93684836-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93684836
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93684836
    reference: chr 14
allele count: 32
allele frequency: 2.742167683553849e-4
allele num: 116696
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*303-37T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.311-37T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.602-37T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.511-37T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.374-37T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.506-37T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.378+3209T>C
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22768
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7127
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14871
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2219
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3245
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3223
  bin: 9.75e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 28026
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2397
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 1
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

14-93684841-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93684841
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93684841
    reference: chr 14
allele count: 1
allele frequency: 8.537959769133568e-6
allele num: 117124
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.378+3214G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*303-32G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.511-32G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.374-32G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.602-32G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.311-32G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.506-32G>A
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25403
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15669
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31426
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1720
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

14-93684842-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93684842
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93684842
    reference: chr 14
allele count: 1
allele frequency: 8.523841183791064e-6
allele num: 117318
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.511-31T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.311-31T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.378+3215T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*303-31T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.374-31T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.602-31T>C
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.506-31T>C
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2444
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25841
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1905
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3211
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2744
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ

14-93684845-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93684845
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93684845
    reference: chr 14
allele count: 9
allele frequency: 7.644870292034045e-5
allele num: 117726
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*303-28G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.506-28G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.602-28G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.378+3218G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.311-28G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.374-28G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.511-28G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7552
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26644
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1731
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16167
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2318
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2770
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 790
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

14-93684871-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93684871
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93684871
    reference: chr 14
allele count: 2
allele frequency: 1.660109235187675e-5
allele num: 120474
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.378+3244A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.374-2A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.602-2A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.506-2A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*303-2A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.311-2A>G
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.511-2A>G
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17736
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37179
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: c.602-2A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

14-93684892-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93684892
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93684892
    reference: chr 14
allele count: 1
allele frequency: 8.270751315049459e-6
allele num: 120908
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*322G>A
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.621G>A
  hgvsp: ENST00000013070.6:c.621G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.525G>A
  hgvsp: ENST00000554232.1:c.525G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.330G>A
  hgvsp: ENST00000556871.1:c.330G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.530G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.393G>A
  hgvsp: ENST00000416753.1:c.393G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.378+3265G>A
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8141
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28992
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 981
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37587
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1208
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2416
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu207Glu
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

14-93684893-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 93684893
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 93684893
    reference: chr 14
allele count: 3
allele frequency: 2.480897092388608e-5
allele num: 120924
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451785
  ensembl transcript: ENST00000553857
  gene symbol: UBR7
  hgvsc: ENST00000553857.1:c.378+3266G>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450470
  ensembl transcript: ENST00000553674
  gene symbol: UBR7
  hgvsc: ENST00000553674.1:c.*323G>T
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000391706
  ensembl transcript: ENST00000416753
  gene symbol: UBR7
  hgvsc: ENST00000416753.1:c.394G>T
  hgvsp: ENSP00000391706.1:p.Asp132Tyr
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000451022
  ensembl transcript: ENST00000556871
  gene symbol: UBR7
  hgvsc: ENST00000556871.1:c.331G>T
  hgvsp: ENSP00000451022.1:p.Asp111Tyr
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000013070
  ensembl transcript: ENST00000013070
  gene symbol: UBR7
  hgvsc: ENST00000013070.6:c.622G>T
  hgvsp: ENSP00000013070.6:p.Asp208Tyr
  variant of: http://identifiers.org/hgnc/20344
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000259066
  ensembl transcript: ENST00000557048
  gene symbol: RP11-371E8.4
  hgvsc: ENST00000557048.1:n.531G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000012963
  ensembl protein: ENSP00000450645
  ensembl transcript: ENST00000554232
  gene symbol: UBR7
  hgvsc: ENST00000554232.1:c.526G>T
  hgvsp: ENSP00000450645.1:p.Asp176Tyr
  variant of: http://identifiers.org/hgnc/20344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28989
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1208
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 982
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp208Tyr
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 504
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1098
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1005
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6976
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 274
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1775
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21948
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3976
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37896
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5136
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.501250625312656e-4
allele num: 11994
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6818
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 642
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.29e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

DP
type: SiteQuality
SIO_000300: 1.216549e6

MQ
type: SiteQuality
SIO_000300: 5.907e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.86e-1

QD
type: SiteQuality
SIO_000300: 1.399e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.96e-1

GenotypeQuality
all individuals: 405
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6979
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1679
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 463
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 462
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13463
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 834
bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
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allele frequency: 0.0e0
allele num: 13604
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 6.130456105934282e-5
allele num: 48936
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8350
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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5402
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9946
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.48e-1

MQRankSum
type: SiteQuality
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VQSLOD
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BaseQRankSum
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DP
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -1.3e-3

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.19e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 50072
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.329080276448698e-4
allele num: 7524
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8522
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10096
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13758
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5512
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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MQ
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DP
type: SiteQuality
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QD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

FS
type: SiteQuality
SIO_000300: 2.593e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10462
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7922
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5830
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.875187518751875e-5
allele num: 53328
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.035e0

MQRankSum
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MQ
type: SiteQuality
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QD
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ClippingRankSum
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DP
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -6.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -7.67e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5890
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14300
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10510
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.858528788610936e-5
allele num: 53806
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
type: SiteQuality
SIO_000300: -2.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.131e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.42e-1

InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 6.304e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.42e-1

DP
type: SiteQuality
SIO_000300: 1.455161e6

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.31e0

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.223990208078335e-4
allele num: 8170
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56262
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.9e1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.487646e6

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
allele num: 14720
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 1.77683013503909e-5
allele num: 56280
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Other
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East Asian
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allele frequency: 0.0e0
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African
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allele num: 9268
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
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QD
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BaseQRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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FS
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VQSLOD
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InbreedingCoeff
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

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

European (Finnish)
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East Asian
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European (Non-Finnish)
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South Asian
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Other
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African
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QD
type: SiteQuality
SIO_000300: 1.469e1

MQRankSum
type: SiteQuality
SIO_000300: 7.5e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

FS
type: SiteQuality
SIO_000300: 5.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.83e-1

DP
type: SiteQuality
SIO_000300: 1.314795e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.226e0

GenotypeQuality
all individuals: 102
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

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

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 3.75e1
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GenotypeQuality
all individuals: 6979
bin: 9.75e1
variant carriers: 3

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8414
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 8.394543546694649e-5
allele num: 47650
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7034
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.99e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

DP
type: SiteQuality
SIO_000300: 1.281287e6

FS
type: SiteQuality
SIO_000300: 3.023e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.145e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 501
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GenotypeQuality
all individuals: 311
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13356
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5160
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9222
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6934
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 720
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.126121529106604e-5
allele num: 47034
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.059e0

VQSLOD
type: SiteQuality
SIO_000300: -4.529e-1

QD
type: SiteQuality
SIO_000300: 8.039999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 3.93e-1

FS
type: SiteQuality
SIO_000300: 3.822e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.45e-1

DP
type: SiteQuality
SIO_000300: 1.263747e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.102e0

GenotypeQuality
all individuals: 211
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 397
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variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44552
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.977600796416127e-4
allele num: 8036
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13022
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8670
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.153e0

QD
type: SiteQuality
SIO_000300: 1.132e1

VQSLOD
type: SiteQuality
SIO_000300: 4.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.09e-1

FS
type: SiteQuality
SIO_000300: 2.674e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

MQ
type: SiteQuality
SIO_000300: 5.922e1

DP
type: SiteQuality
SIO_000300: 1.18824e6

GenotypeQuality
all individuals: 226
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3011
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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
all individuals: 3551
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variant carriers: 0

GenotypeQuality
all individuals: 434
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12728
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 656
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8098
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41866
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.305142260506395e-4
allele num: 7662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6058
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4606
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 4.9e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.662e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e0

VQSLOD
type: SiteQuality
SIO_000300: -1.842e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-3

DP
type: SiteQuality
SIO_000300: 1.108981e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

GenotypeQuality
all individuals: 160
bin: 5.25e1
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
all individuals: 6975
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 904
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 397
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GenotypeQuality
all individuals: 780
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variant carriers: 0

GenotypeQuality
all individuals: 226
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GenotypeQuality
all individuals: 308
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 41076
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4524
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.951653944020357e-5
allele num: 12576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7962
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5958
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.358e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.53e0

VQSLOD
type: SiteQuality
SIO_000300: -2.85e-2

FS
type: SiteQuality
SIO_000300: 5.985e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e0

MQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.926e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 1.093863e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-3

GenotypeQuality
all individuals: 233
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3919
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5772
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6997
bin: 9.75e1
variant carriers: 27

European (Non-Finnish)
type: Population
allele count: 22
allele frequency: 5.596255596255597e-4
allele num: 39312
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4334
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 3.237817710862878e-4
allele num: 12354
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.360174102285093e-4
allele num: 7352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5710
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.14e0

QD
type: SiteQuality
SIO_000300: 1.449e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0

FS
type: SiteQuality
SIO_000300: 3.227e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.999999999999999e-3

DP
type: SiteQuality
SIO_000300: 1.063904e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e-1

GenotypeQuality
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bin: 4.75e1
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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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7126
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.667500416875104e-4
allele num: 11994
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36654
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5290
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4088
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7042
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 584
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.328e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.51e-1

FS
type: SiteQuality
SIO_000300: 4.664e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.24e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.614e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.84e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.7e-1

DP
type: SiteQuality
SIO_000300: 1.02489e6

GenotypeQuality
all individuals: 2600
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4121
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 283
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GenotypeQuality
all individuals: 225
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variant carriers: 0

East Asian
type: Population
allele count: 4
allele frequency: 8.729812309035355e-4
allele num: 4582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6194
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -4.854e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.194e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.58e-2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.8268e5

QD
type: SiteQuality
SIO_000300: 7.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
all individuals: 281
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GenotypeQuality
all individuals: 142
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GenotypeQuality
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GenotypeQuality
all individuals: 390
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GenotypeQuality
all individuals: 533
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GenotypeQuality
all individuals: 4028
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GenotypeQuality
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GenotypeQuality
all individuals: 2393
bin: 6.25e1
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GenotypeQuality
all individuals: 442
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 31182
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.885729518393461e-5
allele num: 11254
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3430
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5872
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 528
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.46e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.62e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.71131e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.315e0

MQRankSum
type: SiteQuality
SIO_000300: -1.102e0

VQSLOD
type: SiteQuality
SIO_000300: -2.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.73e-2

QD
type: SiteQuality
SIO_000300: 1.623e1

GenotypeQuality
all individuals: 3955
bin: 3.25e1
variant carriers: 5

GenotypeQuality
all individuals: 395
bin: 5.25e1
variant carriers: 31

GenotypeQuality
all individuals: 1754
bin: 6.25e1
variant carriers: 8

GenotypeQuality
all individuals: 6870
bin: 1.75e1
variant carriers: 14

GenotypeQuality
all individuals: 655
bin: 4.75e1
variant carriers: 20

GenotypeQuality
all individuals: 3786
bin: 2.75e1
variant carriers: 8

GenotypeQuality
all individuals: 423
bin: 7.75e1
variant carriers: 20

GenotypeQuality
all individuals: 418
bin: 9.25e1
variant carriers: 36

GenotypeQuality
all individuals: 102
bin: 5.75e1
variant carriers: 29

GenotypeQuality
all individuals: 285
bin: 7.25e1
variant carriers: 13

GenotypeQuality
all individuals: 595
bin: 6.75e1
variant carriers: 5

GenotypeQuality
all individuals: 7515
bin: 9.75e1
variant carriers: 639

Other
type: Population
allele count: 11
allele frequency: 2.301255230125523e-2
allele num: 478
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 79
allele frequency: 2.583387835186396e-2
allele num: 3058
num of homozygotes: 1

Latino
type: Population
allele count: 41
allele frequency: 8.401639344262295e-3
allele num: 4880
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 2.056907781967775e-3
allele num: 5834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3620
num of homozygotes: 0

South Asian
type: Population
allele count: 53
allele frequency: 4.897431158750693e-3
allele num: 10822
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 390
allele frequency: 1.411304914236086e-2
allele num: 27634
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.37e-1

QD
type: SiteQuality
SIO_000300: 1.487e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.53e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.48e0

DP
type: SiteQuality
SIO_000300: 9.51412e5

GenotypeQuality
all individuals: 107
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2599
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4563
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4952
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3130
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1205
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4538
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 895
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10890
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.494349915573451e-5
allele num: 15398
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9644
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62024
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.425e0

VQSLOD
type: SiteQuality
SIO_000300: -1.74e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.698e1

DP
type: SiteQuality
SIO_000300: 1.929402e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.81e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e0

GenotypeQuality
all individuals: 179
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3140
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9079
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 754
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1886
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3656
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4856
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variant carriers: 0

GenotypeQuality
all individuals: 273
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variant carriers: 0

GenotypeQuality
all individuals: 2569
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3767
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3901
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15436
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10922
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.608285888899611e-5
allele num: 62178
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.07e-1

DP
type: SiteQuality
SIO_000300: 1.932368e6

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 2.96e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.62e-1

MQ
type: SiteQuality
SIO_000300: 5.744e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.1e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.05e0

GenotypeQuality
all individuals: 193
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2169
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3073
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1115
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2921
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62012
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.493506493506494e-5
allele num: 15400
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10896
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.15e-1

QD
type: SiteQuality
SIO_000300: 1.135e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-2

DP
type: SiteQuality
SIO_000300: 1.962078e6

MQRankSum
type: SiteQuality
SIO_000300: 3.15e-1

GenotypeQuality
all individuals: 261
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4059
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
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variant carriers: 0

GenotypeQuality
all individuals: 3282
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3118
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29713
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variant carriers: 0

GenotypeQuality
all individuals: 1406
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variant carriers: 0

GenotypeQuality
all individuals: 100
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variant carriers: 0

GenotypeQuality
all individuals: 1607
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10964
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.069108214359611e-4
allele num: 9666
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62362
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

QD
type: SiteQuality
SIO_000300: 1.158e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.674e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.84e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.43e-1

DP
type: SiteQuality
SIO_000300: 1.988737e6

FS
type: SiteQuality
SIO_000300: 6.424e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
all individuals: 1316
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3204
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
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variant carriers: 0

GenotypeQuality
all individuals: 685
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variant carriers: 0

GenotypeQuality
all individuals: 339
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variant carriers: 0

GenotypeQuality
all individuals: 319
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variant carriers: 0

GenotypeQuality
all individuals: 117
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variant carriers: 0

GenotypeQuality
all individuals: 3099
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variant carriers: 0

GenotypeQuality
all individuals: 30091
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9076
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6462
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.176193836744295e-4
allele num: 8502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.811547714514835e-5
allele num: 62350
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9666
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.557054320087496e-4
allele num: 10972
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.465795939480151e-5
allele num: 15466
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.247e0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.442e1

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.11e-1

DP
type: SiteQuality
SIO_000300: 1.992885e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e-1

GenotypeQuality
all individuals: 319
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 716
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
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variant carriers: 0

GenotypeQuality
all individuals: 104
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GenotypeQuality
all individuals: 9067
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variant carriers: 1

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 265
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variant carriers: 0

GenotypeQuality
all individuals: 1317
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
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variant carriers: 0

GenotypeQuality
all individuals: 689
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variant carriers: 0

GenotypeQuality
all individuals: 3215
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2998
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10976
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.602769585844339e-5
allele num: 62392
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6460
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15460
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.996256e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.02e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.26e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.0e-1

GenotypeQuality
all individuals: 844
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2509
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2241
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 715
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GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 701
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GenotypeQuality
all individuals: 469
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GenotypeQuality
all individuals: 268
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GenotypeQuality
all individuals: 32429
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variant carriers: 0

GenotypeQuality
all individuals: 116
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variant carriers: 0

GenotypeQuality
all individuals: 3249
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.599744040953447e-5
allele num: 62510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9676
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15488
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.07e-1

FS
type: SiteQuality
SIO_000300: 7.402e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

DP
type: SiteQuality
SIO_000300: 2.01984e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.61e-1

QD
type: SiteQuality
SIO_000300: 1.295e1

GenotypeQuality
all individuals: 419
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9066
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 490
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GenotypeQuality
all individuals: 761
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GenotypeQuality
all individuals: 761
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
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variant carriers: 0

GenotypeQuality
all individuals: 44
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GenotypeQuality
all individuals: 3524
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GenotypeQuality
all individuals: 269
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variant carriers: 0

GenotypeQuality
all individuals: 3484
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variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 9.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15570
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11070
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9746
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.578332649389185e-5
allele num: 63358
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.07394e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.186e-1

QD
type: SiteQuality
SIO_000300: 1.589e1

MQRankSum
type: SiteQuality
SIO_000300: -1.291e0

FS
type: SiteQuality
SIO_000300: 3.695e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.85e-1

GenotypeQuality
all individuals: 40
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 401
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3575
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 481
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3422
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.162520344106022e-4
allele num: 8602
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.832886163280951e-4
allele num: 15654
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.836990595611286e-5
allele num: 63800
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.493978069387021e-4
allele num: 11126
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.34e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.21e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.83e-1

DP
type: SiteQuality
SIO_000300: 2.102596e6

QD
type: SiteQuality
SIO_000300: 1.165e1

GenotypeQuality
all individuals: 505
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 744
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 384
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9064
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3622
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 269
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.999280057595392e-5
allele num: 11112
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63718
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15646
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: -9.279999999999999e-2

FS
type: SiteQuality
SIO_000300: 1.025e0

QD
type: SiteQuality
SIO_000300: 1.664e1

DP
type: SiteQuality
SIO_000300: 2.099156e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.88e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.519e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

GenotypeQuality
all individuals: 113
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 261
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 261
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38315
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.590634344976777e-5
allele num: 62868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15528
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11022
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

VQSLOD
type: SiteQuality
SIO_000300: 4.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.96e-1

FS
type: SiteQuality
SIO_000300: 3.407e0

QD
type: SiteQuality
SIO_000300: 1.079e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 2.083659e6

GenotypeQuality
all individuals: 766
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3189
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8012
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6394
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.04384133611691e-4
allele num: 9580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61346
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10830
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
type: SiteQuality
SIO_000300: 7.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.47e0

MQRankSum
type: SiteQuality
SIO_000300: 8.32e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.544e-1

DP
type: SiteQuality
SIO_000300: 2.039606e6

MQ
type: SiteQuality
SIO_000300: 5.901e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.09e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.02e-1

FS
type: SiteQuality
SIO_000300: 1.378e0

GenotypeQuality
all individuals: 176
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1240
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3265
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 286
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3186
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 298
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1963
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 24
allele frequency: 2.621804675551672e-3
allele num: 9154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57372
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14820
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8114
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.919423900350331e-4
allele num: 10276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6130
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

QD
type: SiteQuality
SIO_000300: 1.524e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

DP
type: SiteQuality
SIO_000300: 1.830773e6

VQSLOD
type: SiteQuality
SIO_000300: 5.98e0

GenotypeQuality
all individuals: 990
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3823
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1573
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1730
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9053
bin: 9.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6090
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9086
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8044
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56754
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14716
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.792351e6

QD
type: SiteQuality
SIO_000300: 1.334e1

VQSLOD
type: SiteQuality
SIO_000300: 8.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

FS
type: SiteQuality
SIO_000300: 6.214e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeQuality
all individuals: 298
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1636
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4161
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1830
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21422
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 474
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13292
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1204
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4389
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.774559909142533e-5
allele num: 56352
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9036
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7998
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6070
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14688
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.666e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.766576e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e0

MQ
type: SiteQuality
SIO_000300: 5.897e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

VQSLOD
type: SiteQuality
SIO_000300: -3.245e-1

QD
type: SiteQuality
SIO_000300: 1.763e1

GenotypeQuality
all individuals: 1405
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3698
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1029
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 818
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6548
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9052
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 118
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5818
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 772
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.025010250102501e-4
allele num: 9756
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14136
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.927e0

FS
type: SiteQuality
SIO_000300: 2.182e0

DP
type: SiteQuality
SIO_000300: 1.660114e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.610000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.66e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

QD
type: SiteQuality
SIO_000300: 1.495e1

GenotypeQuality
all individuals: 295
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6851
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5521
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4511
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4896
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1542
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13206
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.201770223259501e-5
allele num: 45418
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7652
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8956
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.599999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 7.153e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.352e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.88e0

DP
type: SiteQuality
SIO_000300: 1.611775e6

VQSLOD
type: SiteQuality
SIO_000300: 4.15e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.021e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13190
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7646
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8958
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.428571428571429e-3
allele num: 700
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45424
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.611295e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.04e-1

MQ
type: SiteQuality
SIO_000300: 6.04e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

QD
type: SiteQuality
SIO_000300: 1.115e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.14e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10534
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1040
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3146
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.745318352059925e-4
allele num: 8010
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.14e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e-1

QD
type: SiteQuality
SIO_000300: 1.477e1

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.54e-2

DP
type: SiteQuality
SIO_000300: 1.133125e6

VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

MQ
type: SiteQuality
SIO_000300: 6.062e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 13

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3168
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 1.498501498501499e-3
allele num: 8008
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1076
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 256
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 9.389671361502347e-5
allele num: 10650
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.937e1

MQRankSum
type: SiteQuality
SIO_000300: 5.45e-1

QD
type: SiteQuality
SIO_000300: 1.189e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.37e-2

FS
type: SiteQuality
SIO_000300: 3.863e0

VQSLOD
type: SiteQuality
SIO_000300: -6.026e-1

DP
type: SiteQuality
SIO_000300: 1.137262e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.395e0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 165
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 302
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 9.044862518089724e-5
allele num: 11056
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1258
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3258
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8072
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.138e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.78e-1

MQ
type: SiteQuality
SIO_000300: 5.923e1

FS
type: SiteQuality
SIO_000300: 1.388e0

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.481e-1

DP
type: SiteQuality
SIO_000300: 1.164294e6

QD
type: SiteQuality
SIO_000300: 1.325e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.081e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.74e-2

GenotypeQuality
all individuals: 1240
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 209
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GenotypeQuality
all individuals: 89
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 646
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12314
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3584
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 392
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.218620521569583e-4
allele num: 8206
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.154e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.57e-1

DP
type: SiteQuality
SIO_000300: 1.208883e6

MQRankSum
type: SiteQuality
SIO_000300: 3.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.843e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.85e-2

MQ
type: SiteQuality
SIO_000300: 5.944e1

QD
type: SiteQuality
SIO_000300: 1.171e1

FS
type: SiteQuality
SIO_000300: 9.239000000000001e0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.545595054095827e-4
allele num: 12940
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3748
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 438
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1840
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8266
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.227943e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.723e0

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.53e-2

QD
type: SiteQuality
SIO_000300: 2.9e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.166e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.709608158883521e-5
allele num: 14904
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2384
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 270
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8488
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.911e0

FS
type: SiteQuality
SIO_000300: 4.036e0

DP
type: SiteQuality
SIO_000300: 1.266272e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.08e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

QD
type: SiteQuality
SIO_000300: 5.4e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.15e-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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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2414
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15102
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 912
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4220
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.708e0

QD
type: SiteQuality
SIO_000300: 1.185e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 3.833e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.71e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.26e-1

DP
type: SiteQuality
SIO_000300: 1.269668e6

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 241
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GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 912
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2414
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.369668246445498e-4
allele num: 4220
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15102
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.708e0

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

FS
type: SiteQuality
SIO_000300: 3.833e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.71e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.26e-1

QD
type: SiteQuality
SIO_000300: 1.185e1

DP
type: SiteQuality
SIO_000300: 1.269668e6

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 171
bin: 9.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1016
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.339546088500064e-5
allele num: 15774
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 692
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.206e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.88e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.735e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

QD
type: SiteQuality
SIO_000300: 7.4e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.694e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

DP
type: SiteQuality
SIO_000300: 1.282038e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1038
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2678
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 716
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15976
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 296
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.817e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.484e0

MQRankSum
type: SiteQuality
SIO_000300: 2.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.84e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.076e1

VQSLOD
type: SiteQuality
SIO_000300: -2.378e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

DP
type: SiteQuality
SIO_000300: 1.284948e6

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 171
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8926
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 922
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1344
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 308
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.059308072487644e-4
allele num: 4856
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18554
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.619e1

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.53e-2

DP
type: SiteQuality
SIO_000300: 1.322929e6

VQSLOD
type: SiteQuality
SIO_000300: -1.452e0

FS
type: SiteQuality
SIO_000300: 9.228999999999999e0

GenotypeQuality
all individuals: 1605
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4395
bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 170
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4892
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1010
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3298
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.114578689255461e-4
allele num: 8972
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1456
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19134
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 5.992e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.61e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.922e0

FS
type: SiteQuality
SIO_000300: 3.008e0

QD
type: SiteQuality
SIO_000300: 1.249e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.24e-1

DP
type: SiteQuality
SIO_000300: 1.324386e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.49e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.2e-2

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1910
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variant carriers: 0

GenotypeQuality
all individuals: 169
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GenotypeQuality
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GenotypeQuality
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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: 302
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GenotypeQuality
all individuals: 102
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.118818527634818e-4
allele num: 8938
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 948
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 19034
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4846
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1444
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3182
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.86e-1

MQ
type: SiteQuality
SIO_000300: 5.641e1

FS
type: SiteQuality
SIO_000300: 1.494e0

DP
type: SiteQuality
SIO_000300: 1.314311e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.19e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.247e0

QD
type: SiteQuality
SIO_000300: 4.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.76e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.164e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.62e-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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GenotypeQuality
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GenotypeQuality
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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: 89
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variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 3.373819163292847e-4
allele num: 8892
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3054
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4748
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 1.074575542660649e-4
allele num: 18612
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

QD
type: SiteQuality
SIO_000300: 9.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.600000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.63e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.031e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.02e-2

DP
type: SiteQuality
SIO_000300: 1.29779e6

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1218
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2766
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 292
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 17340
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.146000458400183e-4
allele num: 8726
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.25806e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 6.4e-1

QD
type: SiteQuality
SIO_000300: 1.199e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.62e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.96e-1

FS
type: SiteQuality
SIO_000300: 7.475e0

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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1118
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2600
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.05e-2

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 171
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.235191420376606e-5
allele num: 16038
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2484
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1044
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.27e-2

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 3.22e0

QD
type: SiteQuality
SIO_000300: 1.299e1

FS
type: SiteQuality
SIO_000300: 2.315e0

MQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

DP
type: SiteQuality
SIO_000300: 1.220205e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-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
all individuals: 565
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 468
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8438
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2230
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 14338
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3966
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -8.771e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.278e1

DP
type: SiteQuality
SIO_000300: 1.181477e6

ClippingRankSum
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SIO_000300: -1.495e0

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

BaseQRankSum
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SIO_000300: -1.495e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.01e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.5e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8374
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 754
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3846
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 13572
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2098
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

QD
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DP
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.37e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.68e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.73e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 12284
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3570
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8258
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.607717041800643e-3
allele num: 622
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 236
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.175e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e-1

FS
type: SiteQuality
SIO_000300: 2.817e0

DP
type: SiteQuality
SIO_000300: 1.133207e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.99e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

VQSLOD
type: SiteQuality
SIO_000300: -4.903e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1778
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 324
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12164
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 236
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.131515e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.06e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.511e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.38e0

QD
type: SiteQuality
SIO_000300: 1.147e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 13

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 12
allele frequency: 3.382187147688839e-3
allele num: 3548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 232
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1776
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 1.623376623376623e-3
allele num: 616
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.213297743266198e-4
allele num: 8242
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.19e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

QD
type: SiteQuality
SIO_000300: 1.575e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.02e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.130743e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 2.818489289740699e-4
allele num: 3548
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 232
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1776
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8242
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 12116
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.575e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.19e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.02e-2

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.130743e6

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 11096
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8116
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 3350
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1504
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Other
type: Population
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allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: 1.3e0

ClippingRankSum
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SIO_000300: -1.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
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VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 1.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.68e-2

DP
type: SiteQuality
SIO_000300: 1.10081e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15956
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.577137810301864e-5
allele num: 63406
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11154
num of homozygotes: 0

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

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

FS
type: SiteQuality
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ClippingRankSum
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VQSLOD
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MQRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 6.036e1

BaseQRankSum
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63722
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6542
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East Asian
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Latino
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allele frequency: 8.91583452211127e-5
allele num: 11216
num of homozygotes: 0

African
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South Asian
type: Population
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Other
type: Population
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num of homozygotes: 0

FS
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
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VQSLOD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
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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Other
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allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

South Asian
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allele frequency: 6.232082762059081e-5
allele num: 16046
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
type: Population
allele count: 31
allele frequency: 3.7539355776217e-3
allele num: 8258
num of homozygotes: 1

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63964
num of homozygotes: 0

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

DP
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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QD
type: SiteQuality
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1440
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2711
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1164
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7676
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2267
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3209
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9826
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16084
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.206563706563707e-4
allele num: 8288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11292
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.766e0

QD
type: SiteQuality
SIO_000300: 1.131e1

VQSLOD
type: SiteQuality
SIO_000300: -4.41e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 5.903e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.53e-1

DP
type: SiteQuality
SIO_000300: 1.515169e6

GenotypeQuality
all individuals: 953
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31718
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7751
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3353
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1564
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2290
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1169
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.555113212241851e-5
allele num: 64304
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9854
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16098
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.521153e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.92e0

QD
type: SiteQuality
SIO_000300: 1.334e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.56e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 7887
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1263
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33013
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1702
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3225
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 3357
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.078360891445004e-3
allele num: 8346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64554
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9890
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16152
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.0e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.938e0

QD
type: SiteQuality
SIO_000300: 1.121e1

DP
type: SiteQuality
SIO_000300: 1.538023e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.39e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

GenotypeQuality
all individuals: 3243
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3497
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2401
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2873
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8335
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 979
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.022243713733075e-5
allele num: 66176
num of homozygotes: 0

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.003e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

QD
type: SiteQuality
SIO_000300: 1.554e1

DP
type: SiteQuality
SIO_000300: 1.600063e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.958e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.3e-2

GenotypeQuality
all individuals: 3241
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8398
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 65
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3509
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2891
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10294
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: 8636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66458
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: 902
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.070908207867897e-5
allele num: 16472
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 4.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.38e-1

QD
type: SiteQuality
SIO_000300: 1.106e1

MQ
type: SiteQuality
SIO_000300: 5.96e1

VQSLOD
type: SiteQuality
SIO_000300: 8.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

DP
type: SiteQuality
SIO_000300: 1.607416e6

MQRankSum
type: SiteQuality
SIO_000300: 9.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.265e0