14-25101969-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25101969
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25101969
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 17700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-645G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.167+152G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1533C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.203+152G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*126+152G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.203+152G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.305+152G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.203+152G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.204-44G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9637C>T
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9815
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2000
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

14-25101970-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25101970
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25101970
    reference: chr 14
allele count: 1
allele frequency: 5.619240278714318e-5
allele num: 17796
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*126+151G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1532C>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.203+151G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-646G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.204-45G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.305+151G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.167+151G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.203+151G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.203+151G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9638C>G
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34091
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4750
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1278
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

14-25102077-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102077
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102077
    reference: chr 14
allele count: 2
allele frequency: 1.698773485543438e-5
allele num: 117732
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.305+44C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*126+44C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.203+44C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.167+44C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.203+44C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.203+44C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-753C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9745G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.203+44C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1425G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6307
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13659
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1674
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

14-25102088-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102088
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102088
    reference: chr 14
allele count: 1
allele frequency: 8.501088139281828e-6
allele num: 117632
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1414C>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.305+33G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.203+33G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*126+33G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-764G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.203+33G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.203+33G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.167+33G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.203+33G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9756C>G
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13655
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1960
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1206
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2393
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1378
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

14-25102104-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102104
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102104
    reference: chr 14
allele count: 1
allele frequency: 8.464820207218798e-6
allele num: 118136
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-780A>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.203+17A>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9772T>G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.203+17A>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1398T>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*126+17A>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.203+17A>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.305+17A>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.167+17A>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.203+17A>C
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13908
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6635
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5656
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6849
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

14-25102115-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102115
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102115
    reference: chr 14
allele count: 1
allele frequency: 8.449085808915476e-6
allele num: 118356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.305+6G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.203+6G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*126+6G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.167+6G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.203+6G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9783C>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.203+6G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-791G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1387C>T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.203+6G>A
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11757
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1216
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5722
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2577
  bin: 8.75e1
  variant carriers: 0
hgvs: c.203+6G>A
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

14-25102116-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102116
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102116
    reference: chr 14
allele count: 2
allele frequency: 1.68947457340767e-5
allele num: 118380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.203+5G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.167+5G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.203+5G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1386C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-792G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.203+5G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.305+5G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*126+5G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.203+5G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9784C>T
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2155
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 3.75e1
  variant carriers: 0
hgvs: c.203+5G>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

14-25102120-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102120
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102120
    reference: chr 14
allele count: 1
allele frequency: 8.437821691952006e-6
allele num: 118514
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.203+1G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1382C>T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.203+1G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.203+1G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.305+1G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.167+1G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.203+1G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9788C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-796G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*126+1G>A
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14362
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13819
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1960
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
hgvs: c.203+1G>A
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

14-25102134-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102134
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102134
    reference: chr 14
allele count: 1
allele frequency: 8.39630562552477e-6
allele num: 119100
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1368G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.190C>T
  hgvsp: ENSP00000216341.4:p.His64Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.190C>T
  hgvsp: ENSP00000371980.1:p.His64Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.190C>T
  hgvsp: ENSP00000450535.1:p.His64Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.190C>T
  hgvsp: ENSP00000434213.1:p.His64Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.154C>T
  hgvsp: ENSP00000387385.3:p.His52Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9802G>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.292C>T
  hgvsp: ENSP00000371982.1:p.His98Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-810C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*113C>T
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15099
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11839
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His64Tyr
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

14-25102141-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102141
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102141
    reference: chr 14
allele count: 1
allele frequency: 8.370442294170824e-6
allele num: 119468
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1361T>C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.183A>G
  hgvsp: ENST00000554242.1:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.183A>G
  hgvsp: ENST00000526004.1:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*106A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-817A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.183A>G
  hgvsp: ENST00000382540.1:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.285A>G
  hgvsp: ENST00000382542.1:c.285A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.183A>G
  hgvsp: ENST00000216341.4:c.183A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.147A>G
  hgvsp: ENST00000415355.3:c.147A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9809T>C
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6708
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11882
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7086
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr61Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/14-25102144-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102144
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102144
    reference: chr 14
allele count: 1
allele frequency: 8.36372152152822e-6
allele num: 119564
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.180G>T
  hgvsp: ENST00000216341.4:c.180G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.282G>T
  hgvsp: ENST00000382542.1:c.282G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*103G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.180G>T
  hgvsp: ENST00000526004.1:c.180G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.180G>T
  hgvsp: ENST00000554242.1:c.180G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.180G>T
  hgvsp: ENST00000382540.1:c.180G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1358C>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.144G>T
  hgvsp: ENST00000415355.3:c.144G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-820G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9812C>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15665
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6707
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2616
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu60Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

14-25102147-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102147
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102147
    reference: chr 14
allele count: 1
allele frequency: 8.353939717970996e-6
allele num: 119704
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.141G>A
  hgvsp: ENST00000415355.3:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.177G>A
  hgvsp: ENST00000216341.4:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.279G>A
  hgvsp: ENST00000382542.1:c.279G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.177G>A
  hgvsp: ENST00000526004.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9815C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.177G>A
  hgvsp: ENST00000382540.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*100G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.177G>A
  hgvsp: ENST00000554242.1:c.177G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-823G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1355C>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14250
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11921
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15798
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val59Val
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

14-25102149-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102149
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102149
    reference: chr 14
allele count: 2
allele frequency: 1.669114701562291e-5
allele num: 119824
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.175G>A
  hgvsp: ENSP00000450535.1:p.Val59Met
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.139G>A
  hgvsp: ENSP00000387385.3:p.Val47Met
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.277G>A
  hgvsp: ENSP00000371982.1:p.Val93Met
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.175G>A
  hgvsp: ENSP00000434213.1:p.Val59Met
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9817C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*98G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1353C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.175G>A
  hgvsp: ENSP00000371980.1:p.Val59Met
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.175G>A
  hgvsp: ENSP00000216341.4:p.Val59Met
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-825G>A
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7159
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val59Met
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

14-25102151-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102151
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102151
    reference: chr 14
allele count: 1
allele frequency: 8.330695279828055e-6
allele num: 120038
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.173T>A
  hgvsp: ENSP00000371980.1:p.Phe58Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.173T>A
  hgvsp: ENSP00000450535.1:p.Phe58Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-827T>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1351A>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.173T>A
  hgvsp: ENSP00000216341.4:p.Phe58Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*96T>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.275T>A
  hgvsp: ENSP00000371982.1:p.Phe92Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.173T>A
  hgvsp: ENSP00000434213.1:p.Phe58Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9819A>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.137T>A
  hgvsp: ENSP00000387385.3:p.Phe46Tyr
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6719
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5912
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Phe58Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

14-25102152-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102152
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102152
    reference: chr 14
allele count: 1
allele frequency: 8.327088017320342e-6
allele num: 120090
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.172T>A
  hgvsp: ENSP00000434213.1:p.Phe58Ile
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.172T>A
  hgvsp: ENSP00000371980.1:p.Phe58Ile
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.274T>A
  hgvsp: ENSP00000371982.1:p.Phe92Ile
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.172T>A
  hgvsp: ENSP00000450535.1:p.Phe58Ile
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9820A>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.136T>A
  hgvsp: ENSP00000387385.3:p.Phe46Ile
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-828T>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.172T>A
  hgvsp: ENSP00000216341.4:p.Phe58Ile
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*95T>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1350A>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14350
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3717
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11971
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6719
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Phe58Ile
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

14-25102155-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102155
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102155
    reference: chr 14
allele count: 4
allele frequency: 3.328174662606294e-5
allele num: 120186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.271G>A
  hgvsp: ENSP00000371982.1:p.Asp91Asn
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.169G>A
  hgvsp: ENSP00000216341.4:p.Asp57Asn
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9823C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-831G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1347C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.169G>A
  hgvsp: ENSP00000434213.1:p.Asp57Asn
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.169G>A
  hgvsp: ENSP00000450535.1:p.Asp57Asn
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.169G>A
  hgvsp: ENSP00000371980.1:p.Asp57Asn
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*92G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.133G>A
  hgvsp: ENSP00000387385.3:p.Asp45Asn
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11989
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16268
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp57Asn
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

14-25102156-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102156
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102156
    reference: chr 14
allele count: 3
allele frequency: 2.494470590191741e-5
allele num: 120266
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*91C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.168C>A
  hgvsp: ENSP00000434213.1:p.Asp56Glu
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.132C>A
  hgvsp: ENSP00000387385.3:p.Asp44Glu
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.270C>A
  hgvsp: ENSP00000371982.1:p.Asp90Glu
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-832C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1346G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9824G>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.168C>A
  hgvsp: ENSP00000450535.1:p.Asp56Glu
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.168C>A
  hgvsp: ENSP00000371980.1:p.Asp56Glu
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.168C>A
  hgvsp: ENSP00000216341.4:p.Asp56Glu
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14435
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6720
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16160
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp56Glu
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

14-25102160-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102160
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102160
    reference: chr 14
allele count: 90557
allele frequency: 7.476387833955286e-1
allele num: 121124
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.164G>A
  hgvsp: ENSP00000216341.4:p.Arg55Gln
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.164G>A
  hgvsp: ENSP00000371980.1:p.Arg55Gln
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*87G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.266G>A
  hgvsp: ENSP00000371982.1:p.Arg89Gln
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.164G>A
  hgvsp: ENSP00000450535.1:p.Arg55Gln
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.128G>A
  hgvsp: ENSP00000387385.3:p.Arg43Gln
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.164G>A
  hgvsp: ENSP00000434213.1:p.Arg55Gln
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-836G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9828C>T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1342C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.75e1
  variant carriers: 605
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 5.75e1
  variant carriers: 1591
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 6.25e1
  variant carriers: 2168
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 231
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 4245
  bin: 8.25e1
  variant carriers: 4225
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 3.25e1
  variant carriers: 1211
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 6.75e1
  variant carriers: 2775
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 5.25e1
  variant carriers: 1111
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 7.25e1
  variant carriers: 3256
genotype depth: GenotypeDepth
  all individuals: 2224
  bin: 2.25e1
  variant carriers: 1137
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 3.75e1
  variant carriers: 897
genotype depth: GenotypeDepth
  all individuals: 3970
  bin: 7.75e1
  variant carriers: 3955
genotype depth: GenotypeDepth
  all individuals: 21505
  bin: 9.75e1
  variant carriers: 21486
genotype depth: GenotypeDepth
  all individuals: 2329
  bin: 2.75e1
  variant carriers: 1368
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 9.25e1
  variant carriers: 4352
genotype depth: GenotypeDepth
  all individuals: 4492
  bin: 8.75e1
  variant carriers: 4482
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.75e1
  variant carriers: 814
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.25e1
  variant carriers: 759
genotype quality: GenotypeQuality
  all individuals: 646
  bin: 7.75e1
  variant carriers: 286
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.25e1
  variant carriers: 21
hgvs: p.Arg55Gln
num of homozygotes: 34146
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-25102170-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102170
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102170
    reference: chr 14
allele count: 1
allele frequency: 8.261049153242462e-6
allele num: 121050
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*77T>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.118T>C
  hgvsp: ENSP00000387385.3:p.Phe40Leu
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1332A>G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9838A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.256T>C
  hgvsp: ENSP00000371982.1:p.Phe86Leu
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.154T>C
  hgvsp: ENSP00000371980.1:p.Phe52Leu
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.154T>C
  hgvsp: ENSP00000450535.1:p.Phe52Leu
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.154T>C
  hgvsp: ENSP00000216341.4:p.Phe52Leu
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.154T>C
  hgvsp: ENSP00000434213.1:p.Phe52Leu
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-846T>C
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15084
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Phe52Leu
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

14-25102173-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102173
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102173
    reference: chr 14
allele count: 5
allele frequency: 4.130524576621231e-5
allele num: 121050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.151G>A
  hgvsp: ENSP00000371980.1:p.Gly51Ser
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.151G>A
  hgvsp: ENSP00000450535.1:p.Gly51Ser
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.151G>A
  hgvsp: ENSP00000216341.4:p.Gly51Ser
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*74G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.253G>A
  hgvsp: ENSP00000371982.1:p.Gly85Ser
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.151G>A
  hgvsp: ENSP00000434213.1:p.Gly51Ser
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.115G>A
  hgvsp: ENSP00000387385.3:p.Gly39Ser
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1329C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-849G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9841C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2825
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15084
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1205
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6559
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly51Ser
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP

14-25102176-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102176
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102176
    reference: chr 14
allele count: 1
allele frequency: 8.261322141995606e-6
allele num: 121046
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1326C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.148G>C
  hgvsp: ENSP00000371980.1:p.Gly50Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.148G>C
  hgvsp: ENSP00000216341.4:p.Gly50Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.250G>C
  hgvsp: ENSP00000371982.1:p.Gly84Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.148G>C
  hgvsp: ENSP00000434213.1:p.Gly50Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*71G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-852G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.148G>C
  hgvsp: ENSP00000450535.1:p.Gly50Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9844C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.112G>C
  hgvsp: ENSP00000387385.3:p.Gly38Arg
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2826
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3840
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15084
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4391
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly50Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

14-25102177-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102177
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102177
    reference: chr 14
allele count: 3
allele frequency: 2.478560452089426e-5
allele num: 121038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*70C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.147C>T
  hgvsp: ENST00000382540.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.249C>T
  hgvsp: ENST00000382542.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.111C>T
  hgvsp: ENST00000415355.3:c.111C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1325G>A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.147C>T
  hgvsp: ENST00000216341.4:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.147C>T
  hgvsp: ENST00000526004.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.147C>T
  hgvsp: ENST00000554242.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-853C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9845G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15085
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3839
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Cys49Cys
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/14-25102178-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102178
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102178
    reference: chr 14
allele count: 2
allele frequency: 1.652373634726284e-5
allele num: 121038
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1324C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.146G>T
  hgvsp: ENSP00000371980.1:p.Cys49Phe
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*69G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9846C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.146G>T
  hgvsp: ENSP00000434213.1:p.Cys49Phe
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.146G>T
  hgvsp: ENSP00000216341.4:p.Cys49Phe
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.248G>T
  hgvsp: ENSP00000371982.1:p.Cys83Phe
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.146G>T
  hgvsp: ENSP00000450535.1:p.Cys49Phe
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.110G>T
  hgvsp: ENSP00000387385.3:p.Cys37Phe
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-854G>T
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15086
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Cys49Phe
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

14-25102178-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102178
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102178
    reference: chr 14
allele count: 1
allele frequency: 8.261868173631421e-6
allele num: 121038
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.146G>A
  hgvsp: ENSP00000216341.4:p.Cys49Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.146G>A
  hgvsp: ENSP00000371980.1:p.Cys49Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1324C>T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*69G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.110G>A
  hgvsp: ENSP00000387385.3:p.Cys37Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-854G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.146G>A
  hgvsp: ENSP00000450535.1:p.Cys49Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9846C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.146G>A
  hgvsp: ENSP00000434213.1:p.Cys49Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.248G>A
  hgvsp: ENSP00000371982.1:p.Cys83Tyr
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15086
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys49Tyr
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

14-25102181-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102181
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102181
    reference: chr 14
allele count: 1
allele frequency: 8.262141216517673e-6
allele num: 121034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.143G>A
  hgvsp: ENSP00000450535.1:p.Arg48Lys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.143G>A
  hgvsp: ENSP00000434213.1:p.Arg48Lys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.107G>A
  hgvsp: ENSP00000387385.3:p.Arg36Lys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*66G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.245G>A
  hgvsp: ENSP00000371982.1:p.Arg82Lys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9849C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.143G>A
  hgvsp: ENSP00000216341.4:p.Arg48Lys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.143G>A
  hgvsp: ENSP00000371980.1:p.Arg48Lys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-857G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1321C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3839
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4488
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15085
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg48Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/14-25102200-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102200
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102200
    reference: chr 14
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.226G>T
  hgvsp: ENSP00000371982.1:p.Asp76Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.124G>T
  hgvsp: ENSP00000371980.1:p.Asp42Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1302C>A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.124G>T
  hgvsp: ENSP00000434213.1:p.Asp42Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-876G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.88G>T
  hgvsp: ENSP00000387385.3:p.Asp30Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.124G>T
  hgvsp: ENSP00000450535.1:p.Asp42Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.124G>T
  hgvsp: ENSP00000216341.4:p.Asp42Tyr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9868C>A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*47G>T
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15085
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3839
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp42Tyr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

14-25102208-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102208
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102208
    reference: chr 14
allele count: 1
allele frequency: 8.275542461808372e-6
allele num: 120838
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.116T>C
  hgvsp: ENSP00000434213.1:p.Met39Thr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9876A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-884T>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.116T>C
  hgvsp: ENSP00000450535.1:p.Met39Thr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1294A>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.116T>C
  hgvsp: ENSP00000371980.1:p.Met39Thr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.116T>C
  hgvsp: ENSP00000216341.4:p.Met39Thr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.80T>C
  hgvsp: ENSP00000387385.3:p.Met27Thr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.218T>C
  hgvsp: ENSP00000371982.1:p.Met73Thr
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*39T>C
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3839
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15085
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 469
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Met39Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

14-25102228-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102228
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102228
    reference: chr 14
allele count: 3
allele frequency: 2.501959868563708e-5
allele num: 119906
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1274G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.96C>T
  hgvsp: ENST00000526004.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.198C>T
  hgvsp: ENST00000382542.1:c.198C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.96C>T
  hgvsp: ENST00000554242.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.96C>T
  hgvsp: ENST00000216341.4:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-904C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*19C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.96C>T
  hgvsp: ENST00000382540.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.60C>T
  hgvsp: ENST00000415355.3:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9896G>A
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15087
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg32Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum

14-25102229-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102229
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102229
    reference: chr 14
allele count: 1
allele frequency: 8.340561820244212e-6
allele num: 119896
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1273C>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.95G>C
  hgvsp: ENSP00000216341.4:p.Arg32Pro
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.95G>C
  hgvsp: ENSP00000434213.1:p.Arg32Pro
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.59G>C
  hgvsp: ENSP00000387385.3:p.Arg20Pro
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.95G>C
  hgvsp: ENSP00000371980.1:p.Arg32Pro
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.197G>C
  hgvsp: ENSP00000371982.1:p.Arg66Pro
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*18G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-905G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.95G>C
  hgvsp: ENSP00000450535.1:p.Arg32Pro
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9897C>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15088
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg32Pro
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-25102229-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102229
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102229
    reference: chr 14
allele count: 2
allele frequency: 1.668112364048842e-5
allele num: 119896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.197G>A
  hgvsp: ENSP00000371982.1:p.Arg66His
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.95G>A
  hgvsp: ENSP00000371980.1:p.Arg32His
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*18G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1273C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.95G>A
  hgvsp: ENSP00000450535.1:p.Arg32His
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-905G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.95G>A
  hgvsp: ENSP00000434213.1:p.Arg32His
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.95G>A
  hgvsp: ENSP00000216341.4:p.Arg32His
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.59G>A
  hgvsp: ENSP00000387385.3:p.Arg20His
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9897C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15088
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg32His
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-25102230-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102230
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102230
    reference: chr 14
allele count: 8
allele frequency: 6.677350427350428e-5
allele num: 119808
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.196C>T
  hgvsp: ENSP00000371982.1:p.Arg66Cys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.94C>T
  hgvsp: ENSP00000434213.1:p.Arg32Cys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.94C>T
  hgvsp: ENSP00000371980.1:p.Arg32Cys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*17C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-906C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1272G>A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.94C>T
  hgvsp: ENSP00000216341.4:p.Arg32Cys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.58C>T
  hgvsp: ENSP00000387385.3:p.Arg20Cys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.94C>T
  hgvsp: ENSP00000450535.1:p.Arg32Cys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9898G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3900
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15092
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg32Cys
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

14-25102231-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102231
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102231
    reference: chr 14
allele count: 1
allele frequency: 8.351986102295126e-6
allele num: 119732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.93C>A
  hgvsp: ENST00000382540.1:c.93C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.93C>A
  hgvsp: ENST00000554242.1:c.93C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.57C>A
  hgvsp: ENST00000415355.3:c.57C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-907C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*16C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.93C>A
  hgvsp: ENST00000216341.4:c.93C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1271G>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.93C>A
  hgvsp: ENST00000526004.1:c.93C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.195C>A
  hgvsp: ENST00000382542.1:c.195C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9899G>T
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15087
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 592
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser31Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

14-25102232-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102232
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102232
    reference: chr 14
allele count: 1
allele frequency: 8.357011532675915e-6
allele num: 119660
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.194C>T
  hgvsp: ENSP00000371982.1:p.Ser65Phe
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.92C>T
  hgvsp: ENSP00000434213.1:p.Ser31Phe
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*15C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.92C>T
  hgvsp: ENSP00000216341.4:p.Ser31Phe
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.56C>T
  hgvsp: ENSP00000387385.3:p.Ser19Phe
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.92C>T
  hgvsp: ENSP00000450535.1:p.Ser31Phe
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9900G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-908C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.92C>T
  hgvsp: ENSP00000371980.1:p.Ser31Phe
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1270G>A
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15087
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48376
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Ser31Phe
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

14-25102241-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102241
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102241
    reference: chr 14
allele count: 1
allele frequency: 8.418500496691529e-6
allele num: 118786
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.83A>G
  hgvsp: ENSP00000216341.4:p.Lys28Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.47A>G
  hgvsp: ENSP00000387385.3:p.Lys16Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-917A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*6A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9909T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.185A>G
  hgvsp: ENSP00000371982.1:p.Lys62Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.83A>G
  hgvsp: ENSP00000434213.1:p.Lys28Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.83A>G
  hgvsp: ENSP00000371980.1:p.Lys28Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.83A>G
  hgvsp: ENSP00000450535.1:p.Lys28Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1261T>C
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15087
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys28Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-25102246-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102246
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102246
    reference: chr 14
allele count: 1
allele frequency: 8.461955050094773e-6
allele num: 118176
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.78G>C
  hgvsp: ENSP00000216341.4:p.Glu26Asp
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.*1G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.78G>C
  hgvsp: ENSP00000434213.1:p.Glu26Asp
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.78G>C
  hgvsp: ENSP00000371980.1:p.Glu26Asp
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9914C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.42G>C
  hgvsp: ENSP00000387385.3:p.Glu14Asp
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-922G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.180G>C
  hgvsp: ENSP00000371982.1:p.Glu60Asp
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.78G>C
  hgvsp: ENSP00000450535.1:p.Glu26Asp
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1256C>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15086
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1282
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu26Asp
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

14-25102248-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102248
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102248
    reference: chr 14
allele count: 3
allele frequency: 2.543838822372214e-5
allele num: 117932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.40G>A
  hgvsp: ENSP00000387385.3:p.Glu14Lys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.134G>A
  hgvsp: ENST00000530830.1:c.134G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.76G>A
  hgvsp: ENSP00000371980.1:p.Glu26Lys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.76G>A
  hgvsp: ENSP00000434213.1:p.Glu26Lys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.178G>A
  hgvsp: ENSP00000371982.1:p.Glu60Lys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.76G>A
  hgvsp: ENSP00000450535.1:p.Glu26Lys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9916C>T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.76G>A
  hgvsp: ENSP00000216341.4:p.Glu26Lys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-924G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1254C>T
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15087
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3838
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu26Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/14-25102253-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102253
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102253
    reference: chr 14
allele count: 2
allele frequency: 1.704129104820981e-5
allele num: 117362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.71G>T
  hgvsp: ENSP00000434213.1:p.Gly24Val
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.71G>T
  hgvsp: ENSP00000371980.1:p.Gly24Val
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.71G>T
  hgvsp: ENSP00000450535.1:p.Gly24Val
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9921C>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.129G>T
  hgvsp: ENST00000530830.1:c.129G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1249C>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-929G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.173G>T
  hgvsp: ENSP00000371982.1:p.Gly58Val
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.71G>T
  hgvsp: ENSP00000216341.4:p.Gly24Val
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.35G>T
  hgvsp: ENSP00000387385.3:p.Gly12Val
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3837
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15089
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48375
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Gly24Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

14-25102253-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102253
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102253
    reference: chr 14
allele count: 1
allele frequency: 8.520645524104906e-6
allele num: 117362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9921C>G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.71G>C
  hgvsp: ENSP00000216341.4:p.Gly24Ala
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.129G>C
  hgvsp: ENST00000530830.1:c.129G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.71G>C
  hgvsp: ENSP00000434213.1:p.Gly24Ala
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.71G>C
  hgvsp: ENSP00000371980.1:p.Gly24Ala
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1249C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.35G>C
  hgvsp: ENSP00000387385.3:p.Gly12Ala
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.71G>C
  hgvsp: ENSP00000450535.1:p.Gly24Ala
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.173G>C
  hgvsp: ENSP00000371982.1:p.Gly58Ala
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-929G>C
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3837
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15089
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3732
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gly24Ala
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

14-25102257-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102257
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102257
    reference: chr 14
allele count: 12
allele frequency: 1.026430587631511e-4
allele num: 116910
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9925C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.67G>A
  hgvsp: ENSP00000450535.1:p.Gly23Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.67G>A
  hgvsp: ENSP00000434213.1:p.Gly23Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.31G>A
  hgvsp: ENSP00000387385.3:p.Gly11Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-933G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1245C>T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.67G>A
  hgvsp: ENSP00000371980.1:p.Gly23Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.67G>A
  hgvsp: ENSP00000216341.4:p.Gly23Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.169G>A
  hgvsp: ENSP00000371982.1:p.Gly57Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.125G>A
  hgvsp: ENSP00000435084.1:p.Arg42Gln
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3837
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4506
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15094
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 1
hgvs: p.Gly23Arg
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

14-25102258-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102258
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102258
    reference: chr 14
allele count: 3
allele frequency: 2.56647161482394e-5
allele num: 116892
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.30C>T
  hgvsp: ENST00000415355.3:c.30C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1244G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.66C>T
  hgvsp: ENST00000382540.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9926G>A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.66C>T
  hgvsp: ENST00000526004.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-934C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.66C>T
  hgvsp: ENST00000554242.1:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.168C>T
  hgvsp: ENST00000382542.1:c.168C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.124C>T
  hgvsp: ENSP00000435084.1:p.Arg42Trp
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.66C>T
  hgvsp: ENST00000216341.4:c.66C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15085
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4507
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3837
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3355
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg42Trp
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: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

14-25102264-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102264
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102264
    reference: chr 14
allele count: 1
allele frequency: 8.605259534627564e-6
allele num: 116208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.60G>A
  hgvsp: ENST00000526004.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.60G>A
  hgvsp: ENST00000216341.4:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.118G>A
  hgvsp: ENSP00000435084.1:p.Asp40Asn
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9932C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.162G>A
  hgvsp: ENST00000382542.1:c.162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1238C>T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.24G>A
  hgvsp: ENST00000415355.3:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.60G>A
  hgvsp: ENST00000554242.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.60G>A
  hgvsp: ENST00000382540.1:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-940G>A
  variant of: http://identifiers.org/hgnc/4709
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3837
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15085
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2391
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3573
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp40Asn
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

14-25102268-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102268
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102268
    reference: chr 14
allele count: 1
allele frequency: 8.63155350700019e-6
allele num: 115854
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.114G>C
  hgvsp: ENSP00000435084.1:p.Gln38His
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.20G>C
  hgvsp: ENSP00000387385.3:p.Gly7Ala
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.56G>C
  hgvsp: ENSP00000434213.1:p.Gly19Ala
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.56G>C
  hgvsp: ENSP00000216341.4:p.Gly19Ala
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1234C>G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.158G>C
  hgvsp: ENSP00000371982.1:p.Gly53Ala
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-944G>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.56G>C
  hgvsp: ENSP00000371980.1:p.Gly19Ala
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.56G>C
  hgvsp: ENSP00000450535.1:p.Gly19Ala
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9936C>G
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2125
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3574
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3837
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15085
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly19Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum

14-25102269-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102269
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102268
    reference: chr 14
allele count: 1
allele frequency: 8.636771920127133e-6
allele num: 115784
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-946delA
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.56-2delA
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.18delA
  hgvsp: ENSP00000387385.3:p.Glu8ArgfsTer20
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.56-2delA
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.114-2delA
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.56-2delA
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.56-2delA
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1232delT
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.158-2delA
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9938delT
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 930
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15085
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3836
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
hgvs: c.56-2delA
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: CT
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

14-25102274-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102274
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102274
    reference: chr 14
allele count: 1
allele frequency: 8.663859576163989e-6
allele num: 115422
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.56-6C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.14C>A
  hgvsp: ENSP00000387385.3:p.Pro5His
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9942G>T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.56-6C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.56-6C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.56-6C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-950C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.158-6C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1228G>T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.114-6C>A
  variant of: http://identifiers.org/hgnc/4709
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3837
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15083
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro5His
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/14-25102299-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102299
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102299
    reference: chr 14
allele count: 1
allele frequency: 8.840951286358412e-6
allele num: 113110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.56-31G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.56-31G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.114-31G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.7-18G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1203C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9967C>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.56-31G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-975G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.56-31G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.158-31G>T
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2824
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3837
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2117
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15083
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3902
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 589
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP

14-25102303-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102303
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102303
    reference: chr 14
allele count: 63
allele frequency: 5.600497822028624e-4
allele num: 112490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.114-35A>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1199T>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.56-35A>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.56-35A>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-979A>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.158-35A>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.56-35A>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.7-22A>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9971T>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.56-35A>T
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1423
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3904
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3575
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4505
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3837
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15111
  bin: 9.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 1553
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1742
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 3.25e1
  variant carriers: 1
num of homozygotes: 1
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

14-25102305-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102305
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102305
    reference: chr 14
allele count: 1
allele frequency: 8.888572850743085e-6
allele num: 112504
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.114-37C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.56-37C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.56-37C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-981C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.56-37C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1197G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.56-37C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.7-24C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.158-37C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9973G>A
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15084
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2649
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4511
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1683
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3842
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

14-25102316-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102316
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102316
    reference: chr 14
allele count: 1
allele frequency: 8.953192708519857e-6
allele num: 111692
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.7-35C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9984G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-992C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.56-48C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.56-48C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.158-48C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.114-48C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.56-48C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1186G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.56-48C>T
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15085
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1925
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2098
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

14-25102316-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102316
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102316
    reference: chr 14
allele count: 1
allele frequency: 8.953192708519857e-6
allele num: 111692
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.56-48C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.56-48C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.56-48C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1186G>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.56-48C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.56-992C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.114-48C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9984G>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.7-35C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.158-48C>A
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15085
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 663
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

14-25102320-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102320
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102320
    reference: chr 14
allele count: 2
allele frequency: 1.793657626632228e-5
allele num: 111504
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.56-52C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.56-52C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1182G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.56-52C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.114-52C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.158-52C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9988G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.7-39C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+992C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.56-52C>T
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3903
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15084
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48366
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD

14-25102330-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25102330
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25102330
    reference: chr 14
allele count: 1
allele frequency: 9.007061536244416e-6
allele num: 111024
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+982T>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.114-62T>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.56-62T>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.56-62T>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-1172A>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.158-62T>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.7-49T>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.56-62T>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+9998A>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.56-62T>A
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2823
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4510
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2870
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4392
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3905
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15083
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 765
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum

14-25103092-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103092
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103092
    reference: chr 14
allele count: 1
allele frequency: 2.695417789757413e-4
allele num: 3710
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+220G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10760C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+220G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+220G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+220G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+220G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.113+24G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+220G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-410C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+220G>A
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7416
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 600
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

14-25103104-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103104
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103104
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 4360
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-398G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+208C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+208C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.113+12C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+208C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+208C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+208C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+208C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+208C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10772G>A
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7332
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

14-25103111-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103111
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103111
    reference: chr 14
allele count: 1
allele frequency: 2.111486486486487e-4
allele num: 4736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+201G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+201G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-391C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+201G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.113+5G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10779C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+201G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+201G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+201G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+201G>A
  variant of: http://identifiers.org/hgnc/4709
canonical: false
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7474
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 580
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 1.75e1
  variant carriers: 0
hgvs: c.113+5G>A
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

14-25103128-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103128
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103128
    reference: chr 14
allele count: 1
allele frequency: 1.45900204260286e-4
allele num: 6854
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+184T>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+184T>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+184T>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+184T>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+184T>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.101T>C
  hgvsp: ENSP00000435084.1:p.Leu34Pro
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+184T>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-374A>G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+184T>C
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10796A>G
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9054
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1518
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8169
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu34Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

14-25103164-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103164
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103164
    reference: chr 14
allele count: 1
allele frequency: 8.254911672445105e-5
allele num: 12114
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+148A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+148A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+148A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+148A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+148A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+148A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-338T>C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.65A>G
  hgvsp: ENSP00000435084.1:p.Lys22Arg
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+148A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10832T>C
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18008
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys22Arg
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

14-25103181-T-TG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103181
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103182
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 13728
alternate allele: TG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+130dupC
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+130dupC
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+130dupC
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.47dupC
  hgvsp: ENSP00000435084.1:p.Ser17LysfsTer6
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-315dupG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10855dupG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+130dupC
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+130dupC
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+130dupC
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+130dupC
  variant of: http://identifiers.org/hgnc/4709
canonical: false
consequence: frameshift
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23689
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser17LysfsTer6
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

14-25103184-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103184
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103184
    reference: chr 14
allele count: 6
allele frequency: 4.199328107502799e-4
allele num: 14288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+128C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-318G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+128C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+128C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.45C>T
  hgvsp: ENST00000530830.1:c.45C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+128C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10852G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+128C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+128C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+128C>T
  variant of: http://identifiers.org/hgnc/4709
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24699
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1798
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro15Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

14-25103220-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103220
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103220
    reference: chr 14
allele count: 1
allele frequency: 5.412426932236415e-5
allele num: 18476
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+92A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.9A>G
  hgvsp: ENST00000530830.1:c.9A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+92A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10888T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+92A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+92A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-282T>C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+92A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+92A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+92A>G
  variant of: http://identifiers.org/hgnc/4709
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32479
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 906
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30668
  bin: 7.5e0
  variant carriers: 0
hgvs: c.9A>G
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

14-25103222-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103222
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103222
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 18464
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+90G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+90G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+90G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+90G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.7G>A
  hgvsp: ENSP00000435084.1:p.Glu3Lys
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+90G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10890C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+90G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-280C>T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+90G>A
  variant of: http://identifiers.org/hgnc/4709
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 32443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8729
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu3Lys
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

14-25103239-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103239
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103239
    reference: chr 14
allele count: 1
allele frequency: 4.981568197668626e-5
allele num: 20074
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+73A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+73A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+73A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.7-17A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-263T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10907T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+73A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+73A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+73A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+73A>G
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30234
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28686
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

14-25103250-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103250
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103250
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 21910
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-252G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+62C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+62C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+62C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.7-28C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10918G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+62C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+62C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+62C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+62C>T
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26816
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 984
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

14-25103252-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103252
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103252
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 22246
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+60C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+60C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+60C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+60C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-250G>T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10920G>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.7-30C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+60C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+60C>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+60C>A
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19671
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1403
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

14-25103267-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103267
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103267
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 26170
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-235C>T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+45G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+45G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+45G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+45G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+45G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.6+45G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+45G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+45G>A
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10935C>T
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7001
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2992
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25246
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1099
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

14-25103269-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103269
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103269
    reference: chr 14
allele count: 1
allele frequency: 3.699045646223274e-5
allele num: 27034
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+43C>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.6+43C>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+43C>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+43C>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+43C>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+43C>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+43C>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+43C>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10937G>C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-233G>C
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25977
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23703
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

14-25103275-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103275
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103275
    reference: chr 14
allele count: 1
allele frequency: 3.41740140796938e-5
allele num: 29262
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+37A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+37A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+37A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+37A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-227T>C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10943T>C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+37A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.6+37A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+37A>G
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+37A>G
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27451
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16916
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3161
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25606
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

14-25103276-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103276
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103276
    reference: chr 14
allele count: 0
allele frequency: 0.0e0
allele num: 29632
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+36C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.6+36C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+36C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+36C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-226G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+36C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+36C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+36C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10944G>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+36C>T
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 8303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27690
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16522
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25944
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

14-25103282-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103282
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103282
    reference: chr 14
allele count: 1
allele frequency: 3.145445395067942e-5
allele num: 31792
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+30C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+30C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+30C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+30C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+30C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10950G>A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+30C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.6+30C>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-220G>A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+30C>T
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28507
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14718
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14094
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 651
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25543
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/14-25103285-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 25103285
    reference: chr 14
  end: Position
    type: ExactPosition
    position: 25103285
    reference: chr 14
allele count: 1
allele frequency: 3.044510747122937e-5
allele num: 32846
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371982
  ensembl transcript: ENST00000382542
  gene symbol: GZMB
  hgvsc: ENST00000382542.1:c.157+27G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000450535
  ensembl transcript: ENST00000554242
  gene symbol: GZMB
  hgvsc: ENST00000554242.1:c.55+27G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000216341
  ensembl transcript: ENST00000216341
  gene symbol: GZMB
  hgvsc: ENST00000216341.4:c.55+27G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000371980
  ensembl transcript: ENST00000382540
  gene symbol: GZMB
  hgvsc: ENST00000382540.1:c.55+27G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000557736
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000557736.1:n.440-217C>A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000258657
  ensembl transcript: ENST00000555300
  gene symbol: RP11-104E19.1
  hgvsc: ENST00000555300.1:n.177+10953C>A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000387385
  ensembl transcript: ENST00000415355
  gene symbol: GZMB
  hgvsc: ENST00000415355.3:c.6+27G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000432074
  ensembl transcript: ENST00000532263
  gene symbol: GZMB
  hgvsc: ENST00000532263.1:c.55+27G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000435084
  ensembl transcript: ENST00000530830
  gene symbol: GZMB
  hgvsc: ENST00000530830.1:c.6+27G>T
  variant of: http://identifiers.org/hgnc/4709
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100453
  ensembl protein: ENSP00000434213
  ensembl transcript: ENST00000526004
  gene symbol: GZMB
  hgvsc: ENST00000526004.1:c.55+27G>T
  variant of: http://identifiers.org/hgnc/4709
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13885
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28729
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 7496
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31937
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1437
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 485
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4751
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 7.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 424
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1656
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7994
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1154
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -6.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.94e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.38e0

MQ
type: SiteQuality
SIO_000300: 5.682e1

QD
type: SiteQuality
SIO_000300: 1.296e1

DP
type: SiteQuality
SIO_000300: 5.29034e5

GenotypeQuality
all individuals: 361
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 281
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7921
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32022
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1780
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 868
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 279
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5928
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1160
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 394
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.336448598130841e-3
allele num: 428
num of homozygotes: 0

South 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: 1664
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.32394e5

MQRankSum
type: SiteQuality
SIO_000300: 1.25e-1

MQ
type: SiteQuality
SIO_000300: 5.868e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.15e-2

FS
type: SiteQuality
SIO_000300: 1.0639e1

QD
type: SiteQuality
SIO_000300: 5.09e0

VQSLOD
type: SiteQuality
SIO_000300: -1.375e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.279e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e0

GenotypeQuality
all individuals: 216
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2467
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5058
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1196
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1722
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3287
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4491
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6139
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11053
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3343
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2270
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.044418059487929e-5
allele num: 65694
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14244
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.9e-2

DP
type: SiteQuality
SIO_000300: 1.789128e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.753e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: 3.92e-1

FS
type: SiteQuality
SIO_000300: 5.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.21e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

QD
type: SiteQuality
SIO_000300: 1.597e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 477
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5291
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2369
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6511
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1061
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13030
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1082
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 229
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4747
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13740
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3447
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3490
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521977352976988e-5
allele num: 65704
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10348
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14100
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.838e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.147e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e-1

QD
type: SiteQuality
SIO_000300: 1.458e1

DP
type: SiteQuality
SIO_000300: 1.818106e6

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

GenotypeQuality
all individuals: 559
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13634
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 3779
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 856
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3619
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2195
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5111
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13963
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2548
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517082347229808e-5
allele num: 65916
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14232
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.987e0

MQRankSum
type: SiteQuality
SIO_000300: 2.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.5e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.478e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.134e1

DP
type: SiteQuality
SIO_000300: 1.850438e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.331e0

VQSLOD
type: SiteQuality
SIO_000300: 3.0e-2

GenotypeQuality
all individuals: 143
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 757
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5158
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6877
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3653
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
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variant carriers: 0

GenotypeQuality
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 117
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variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3803
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14002
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 127
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
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variant carriers: 0

GenotypeQuality
all individuals: 2045
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13930
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65988
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.633911368015414e-5
allele num: 10380
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.492e0

QD
type: SiteQuality
SIO_000300: 1.521e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.125e0

FS
type: SiteQuality
SIO_000300: 2.541e0

DP
type: SiteQuality
SIO_000300: 1.85934e6

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14008
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 6883
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2047
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
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variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5161
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
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variant carriers: 0

GenotypeQuality
all individuals: 2576
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5726
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3653
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3807
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14004
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.029935765361774e-5
allele num: 66008
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14328
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.169e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.94e-1

DP
type: SiteQuality
SIO_000300: 1.860188e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

QD
type: SiteQuality
SIO_000300: 1.526e1

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

GenotypeQuality
all individuals: 2585
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515105602860519e-5
allele num: 66002
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14462
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.64e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e0

VQSLOD
type: SiteQuality
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DP
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SIO_000300: 1.863518e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.58e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.192e1

GenotypeQuality
all individuals: 1598
bin: 2.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511030522816561e-5
allele num: 66180
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14826
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.833e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.329e0

QD
type: SiteQuality
SIO_000300: 1.195e1

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.23e-1

VQSLOD
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SIO_000300: 2.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.76e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

DP
type: SiteQuality
SIO_000300: 1.878117e6

GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66260
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -8.531e-1

DP
type: SiteQuality
SIO_000300: 1.885735e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.57e-1

FS
type: SiteQuality
SIO_000300: 6.849e0

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.56e0

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.749e1

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
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: 8646
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50879628232596e-5
allele num: 66278
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.64e-1

FS
type: SiteQuality
SIO_000300: 1.415e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.247e0

VQSLOD
type: SiteQuality
SIO_000300: -8.999999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-1

DP
type: SiteQuality
SIO_000300: 1.888819e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.82e-1

MQ
type: SiteQuality
SIO_000300: 5.872e1

QD
type: SiteQuality
SIO_000300: 1.003e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

Other
type: Population
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: 15260
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66322
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.076e1

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

DP
type: SiteQuality
SIO_000300: 1.892156e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.61e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.741e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.414e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.73e-1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15358
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.014681498899641e-5
allele num: 66342
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
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Other
type: Population
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allele num: 894
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FS
type: SiteQuality
SIO_000300: 5.639999999999999e-1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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SIO_000300: -5.212e0

VQSLOD
type: SiteQuality
SIO_000300: 2.1e-1

MQRankSum
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.82e-1

DP
type: SiteQuality
SIO_000300: 1.894847e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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allele count: 1
allele frequency: 1.506432466632521e-5
allele num: 66382
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
type: Population
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.03e-1

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 3.1055e1

DP
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
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South Asian
type: Population
allele count: 1
allele frequency: 6.425083526085839e-5
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MQRankSum
type: SiteQuality
SIO_000300: -3.89e-1

DP
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.97e1

VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3692
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2628
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 2.25e1
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GenotypeQuality
all individuals: 19
bin: 7.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3953
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7255
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66410
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.278772378516624e-4
allele num: 15640
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.728608470181504e-4
allele num: 11570
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

FS
type: SiteQuality
SIO_000300: 1.516e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

QD
type: SiteQuality
SIO_000300: 1.272e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.104e0

VQSLOD
type: SiteQuality
SIO_000300: 2.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.25e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

DP
type: SiteQuality
SIO_000300: 1.901843e6

GenotypeQuality
all individuals: 7283
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5943
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 14133
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 201
bin: 2.75e1
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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
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505343971097396e-5
allele num: 66430
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.273885350318471e-4
allele num: 15700
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.903363e6

QD
type: SiteQuality
SIO_000300: 1.172e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.164e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

FS
type: SiteQuality
SIO_000300: 1.4134e1

MQRankSum
type: SiteQuality
SIO_000300: -5.649999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-2

MQ
type: SiteQuality
SIO_000300: 5.938e1

VQSLOD
type: SiteQuality
SIO_000300: -1.902e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e-1

GenotypeQuality
all individuals: 66
bin: 4.25e1
variant carriers: 56

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 13

GenotypeQuality
all individuals: 170
bin: 5.25e1
variant carriers: 155

GenotypeQuality
all individuals: 1431
bin: 6.25e1
variant carriers: 229

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 8
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variant carriers: 5

GenotypeQuality
all individuals: 120
bin: 4.75e1
variant carriers: 109

GenotypeQuality
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bin: 5.75e1
variant carriers: 94

GenotypeQuality
all individuals: 402
bin: 7.25e1
variant carriers: 165

GenotypeQuality
all individuals: 60
bin: 3.25e1
variant carriers: 39

GenotypeQuality
all individuals: 67
bin: 3.75e1
variant carriers: 48

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 5

GenotypeQuality
all individuals: 755
bin: 6.75e1
variant carriers: 274

GenotypeQuality
all individuals: 55195
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variant carriers: 54185

GenotypeQuality
all individuals: 640
bin: 8.25e1
variant carriers: 335

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 9

GenotypeQuality
all individuals: 538
bin: 9.25e1
variant carriers: 279

GenotypeQuality
all individuals: 332
bin: 8.75e1
variant carriers: 166

European (Finnish)
type: Population
allele count: 5311
allele frequency: 8.032365396249244e-1
allele num: 6612
num of homozygotes: 2121

Other
type: Population
allele count: 686
allele frequency: 7.555066079295154e-1
allele num: 908
num of homozygotes: 259

European (Non-Finnish)
type: Population
allele count: 51093
allele frequency: 7.666096507021967e-1
allele num: 66648
num of homozygotes: 19599

African
type: Population
allele count: 6052
allele frequency: 5.821469796075414e-1
allele num: 10396
num of homozygotes: 1755

East Asian
type: Population
allele count: 6373
allele frequency: 7.372744099953725e-1
allele num: 8644
num of homozygotes: 2360

Latino
type: Population
allele count: 9823
allele frequency: 8.488593155893536e-1
allele num: 11572
num of homozygotes: 4192

South Asian
type: Population
allele count: 11219
allele frequency: 6.86429270680372e-1
allele num: 16344
num of homozygotes: 3860

DP
type: SiteQuality
SIO_000300: 5.050422e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.59e-1

QD
type: SiteQuality
SIO_000300: 2.653e1

FS
type: SiteQuality
SIO_000300: 5.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.99e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.808e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.66e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.04e-1

GenotypeQuality
all individuals: 631
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 376
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variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 1.25e1
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GenotypeQuality
all individuals: 6507
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variant carriers: 0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 28
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GenotypeQuality
all individuals: 115
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variant carriers: 0

GenotypeQuality
all individuals: 289
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variant carriers: 0

GenotypeQuality
all individuals: 107
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variant carriers: 0

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

GenotypeQuality
all individuals: 593
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1754
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 851
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variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48402
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.02e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.92e-1

FS
type: SiteQuality
SIO_000300: 1.5818e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.702e0

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 5.5e0

DP
type: SiteQuality
SIO_000300: 4.507968e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e0

GenotypeQuality
all individuals: 70
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 112
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variant carriers: 0

GenotypeQuality
all individuals: 61
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 372
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variant carriers: 0

GenotypeQuality
all individuals: 291
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variant carriers: 0

GenotypeQuality
all individuals: 111
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 104
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GenotypeQuality
all individuals: 842
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variant carriers: 0

GenotypeQuality
all individuals: 646
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GenotypeQuality
all individuals: 48402
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 624
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 113
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variant carriers: 0

GenotypeQuality
all individuals: 1740
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

East Asian
type: Population
allele count: 5
allele frequency: 5.777675063554426e-4
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16282
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.217e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 7.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.633e0

FS
type: SiteQuality
SIO_000300: 6.709e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

MQRankSum
type: SiteQuality
SIO_000300: 8.9e-2

DP
type: SiteQuality
SIO_000300: 4.508209e6

GenotypeQuality
all individuals: 368
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variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.25e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 101
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GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 622
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 641
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variant carriers: 0

GenotypeQuality
all individuals: 590
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GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

QD
type: SiteQuality
SIO_000300: 1.177e1

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

MQRankSum
type: SiteQuality
SIO_000300: 3.39e-1

FS
type: SiteQuality
SIO_000300: 2.371e0

DP
type: SiteQuality
SIO_000300: 4.508397e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.002e0

GenotypeQuality
all individuals: 639
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1732
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variant carriers: 0

GenotypeQuality
all individuals: 297
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GenotypeQuality
all individuals: 36
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GenotypeQuality
all individuals: 93
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GenotypeQuality
all individuals: 5
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 5
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GenotypeQuality
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GenotypeQuality
all individuals: 108
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GenotypeQuality
all individuals: 90
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 367
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GenotypeQuality
all individuals: 48394
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variant carriers: 3

GenotypeQuality
all individuals: 6698
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variant carriers: 0

GenotypeQuality
all individuals: 64
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GenotypeQuality
all individuals: 832
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 1.923076923076923e-4
allele num: 10400
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.140997297961189e-5
allele num: 16284
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.411e1

FS
type: SiteQuality
SIO_000300: 5.468e0

MQRankSum
type: SiteQuality
SIO_000300: -3.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.86e-1

DP
type: SiteQuality
SIO_000300: 4.508532e6

MQ
type: SiteQuality
SIO_000300: 5.97e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 101
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GenotypeQuality
all individuals: 291
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GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 41
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 48391
bin: 9.75e1
variant carriers: 2

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16274
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501231009427731e-5
allele num: 66612
num of homozygotes: 0

QD
type: SiteQuality
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.958e1

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-1

DP
type: SiteQuality
SIO_000300: 4.508492e6

FS
type: SiteQuality
SIO_000300: 3.729e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e0

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 1.501231009427731e-5
allele num: 66612
num of homozygotes: 0

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

Other
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FS
type: SiteQuality
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ClippingRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 1.0e-4

MQ
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MQRankSum
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VQSLOD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.501366243281386e-5
allele num: 66606
num of homozygotes: 0

QD
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SIO_000300: 1.38e1

ReadPosRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -2.107e0

DP
type: SiteQuality
SIO_000300: 4.508643e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.84e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

African
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allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.571e0

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.904e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.48e-1

VQSLOD
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MQ
type: SiteQuality
SIO_000300: 5.943e1

InbreedingCoeff
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SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.8e-2

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 4.508353e6

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

East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
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 count: 0
allele frequency: 0.0e0
allele num: 66562
num of homozygotes: 0

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

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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ReadPosRankSum
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FS
type: SiteQuality
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MQ
type: SiteQuality
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DP
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MQRankSum
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QD
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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SIO_000300: 1.21e0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.521749615651282e-5
allele num: 66346
num of homozygotes: 0

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

Other
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South Asian
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African
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Latino
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European (Non-Finnish)
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European (Finnish)
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DP
type: SiteQuality
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MQRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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QD
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FS
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MQ
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InbreedingCoeff
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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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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

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

South Asian
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Latino
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European (Finnish)
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allele frequency: 1.209555488358028e-3
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66314
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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FS
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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QD
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MQ
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SIO_000300: 5.969e1

GenotypeQuality
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variant carriers: 1

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

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

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

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

Latino
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European (Non-Finnish)
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allele frequency: 1.508705229172324e-5
allele num: 66282
num of homozygotes: 0

South Asian
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VQSLOD
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MQRankSum
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DP
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FS
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MQ
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SIO_000300: 5.954e1

QD
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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SIO_000300: -7.64e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10370
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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.514784294716432e-5
allele num: 66016
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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South Asian
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MQRankSum
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SIO_000300: -1.584e0

QD
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ClippingRankSum
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SIO_000300: 1.11e0

VQSLOD
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MQ
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SIO_000300: 5.815e1

DP
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FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -3.0e-4

ReadPosRankSum
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BaseQRankSum
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SIO_000300: -5.4e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.518326197200206e-5
allele num: 65862
num of homozygotes: 0

South Asian
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Other
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allele frequency: 0.0e0
allele num: 866
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European (Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.097e0

DP
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ClippingRankSum
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QD
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VQSLOD
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ReadPosRankSum
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MQRankSum
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MQ
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SIO_000300: 5.917e1

FS
type: SiteQuality
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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allele num: 65790
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East Asian
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Other
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South Asian
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Latino
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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ReadPosRankSum
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FS
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VQSLOD
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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African
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European (Non-Finnish)
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Other
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South Asian
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Latino
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MQ
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FS
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DP
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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European (Finnish)
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South Asian
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European (Non-Finnish)
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East Asian
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ClippingRankSum
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ReadPosRankSum
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FS
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QD
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VQSLOD
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DP
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BaseQRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.67305088024763e-5
allele num: 10338
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.491201908738443e-4
allele num: 13412
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.068441296782465e-4
allele num: 65516
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.173708920187793e-3
allele num: 852
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.957e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.54e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.228e1

VQSLOD
type: SiteQuality
SIO_000300: 2.88e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.03e-1

DP
type: SiteQuality
SIO_000300: 4.445242e6

GenotypeQuality
all individuals: 385
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 7.467144563918757e-5
allele num: 13392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.052596233096249e-5
allele num: 65518
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

FS
type: SiteQuality
SIO_000300: 1.755e0

QD
type: SiteQuality
SIO_000300: 1.056e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.444362e6

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531299767242435e-5
allele num: 65304
num of homozygotes: 0

East Asian
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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: 12952
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 9.75e-1

DP
type: SiteQuality
SIO_000300: 4.437741e6

MQRankSum
type: SiteQuality
SIO_000300: -2.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.31e0

QD
type: SiteQuality
SIO_000300: 1.38e1

FS
type: SiteQuality
SIO_000300: 2.396e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.421e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.603e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

GenotypeQuality
all individuals: 39
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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 3667
bin: 2.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 7.878978884336589e-5
allele num: 12692
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65218
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.07e-1

FS
type: SiteQuality
SIO_000300: 7.754e0

DP
type: SiteQuality
SIO_000300: 4.434465e6

QD
type: SiteQuality
SIO_000300: 1.064e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.862e0

GenotypeQuality
all individuals: 738
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1109
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variant carriers: 0

GenotypeQuality
all individuals: 591
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 48372
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GenotypeQuality
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GenotypeQuality
all individuals: 30
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GenotypeQuality
all individuals: 359
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variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65204
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12636
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.686168151879117e-5
allele num: 10324
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.59e-1

QD
type: SiteQuality
SIO_000300: 1.264e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

FS
type: SiteQuality
SIO_000300: 5.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.669e0

DP
type: SiteQuality
SIO_000300: 4.433766e6

MQ
type: SiteQuality
SIO_000300: 6.052e1

GenotypeQuality
all individuals: 357
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variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12360
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.691800736576855e-5
allele num: 10318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65130
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -9.19e-1

DP
type: SiteQuality
SIO_000300: 4.429987e6

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

MQ
type: SiteQuality
SIO_000300: 5.572e1

QD
type: SiteQuality
SIO_000300: 1.037e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.3e-2

VQSLOD
type: SiteQuality
SIO_000300: -4.846e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.02e-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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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64532
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
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: 8600
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Latino
type: Population
allele count: 1
allele frequency: 8.686587908269631e-5
allele num: 11512
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.002e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
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SIO_000300: -5.057e0

InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 3.12e-1

DP
type: SiteQuality
SIO_000300: 4.410117e6

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

Latino
type: Population
allele count: 1
allele frequency: 8.698677800974252e-5
allele num: 11496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

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

South Asian
type: Population
allele count: 16
allele frequency: 1.541425818882466e-3
allele num: 10380
num of homozygotes: 1

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
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European (Non-Finnish)
type: Population
allele count: 46
allele frequency: 7.146852277670748e-4
allele num: 64364
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.407483e6

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
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FS
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BaseQRankSum
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SIO_000300: 1.94e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.57e-1

QD
type: SiteQuality
SIO_000300: 1.387e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.36e0

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

European (Non-Finnish)
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allele frequency: 1.553470452991984e-5
allele num: 64372
num of homozygotes: 0

Other
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num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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QD
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FS
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MQ
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VQSLOD
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DP
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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allele num: 802
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African
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East Asian
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FS
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MQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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DP
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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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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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.558214909000249e-5
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num of homozygotes: 0

African
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South Asian
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Latino
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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DP
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FS
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MQ
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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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

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

East Asian
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South Asian
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MQRankSum
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SIO_000300: -4.06e-1

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

Other
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South Asian
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African
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Latino
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.562793023691942e-5
allele num: 63988
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
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BaseQRankSum
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MQ
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

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

South Asian
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BaseQRankSum
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InbreedingCoeff
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MQ
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QD
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VQSLOD
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FS
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MQRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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Latino
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South Asian
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European (Non-Finnish)
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African
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Other
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FS
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BaseQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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QD
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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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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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bin: 6.75e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 2566
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.930501930501931e-3
allele num: 518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3294
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.727e0

QD
type: SiteQuality
SIO_000300: 1.328e1

VQSLOD
type: SiteQuality
SIO_000300: -1.474e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.99e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.23e-1

DP
type: SiteQuality
SIO_000300: 1.16745e5

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 936
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.152389151958674e-4
allele num: 4646
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 12
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 402
num of homozygotes: 0

QD
type: SiteQuality
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MQRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: -6.88e-2

MQ
type: SiteQuality
SIO_000300: 5.92e1

ClippingRankSum
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SIO_000300: -1.069e0

FS
type: SiteQuality
SIO_000300: 1.455e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.89e-1

DP
type: SiteQuality
SIO_000300: 1.93814e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 22
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 140
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6076
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.054e1

QD
type: SiteQuality
SIO_000300: 1.17e0

DP
type: SiteQuality
SIO_000300: 2.23658e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.439999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.95e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.5e-1

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 1.016260162601626e-3
allele num: 5904
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6128
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1352
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.32032e5

BaseQRankSum
type: SiteQuality
SIO_000300: -6.37e-1

QD
type: SiteQuality
SIO_000300: 1.374e1

MQRankSum
type: SiteQuality
SIO_000300: -5.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.26e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.11e-1

FS
type: SiteQuality
SIO_000300: 2.511e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.76e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2650
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.214771622934888e-4
allele num: 8232
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 172
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.83e-1

BaseQRankSum
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SIO_000300: 3.55e0

DP
type: SiteQuality
SIO_000300: 3.18675e5

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.900000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.327e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 384
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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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: 170
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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MQRankSum
type: SiteQuality
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VQSLOD
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QD
type: SiteQuality
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ReadPosRankSum
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DP
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SIO_000300: 3.22732e5

ClippingRankSum
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SIO_000300: -7.31e-1

FS
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 100
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

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

East Asian
type: Population
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allele frequency: 0.0e0
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Other
type: Population
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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: 6502
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.106439477760567e-4
allele num: 9038
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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QD
type: SiteQuality
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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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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 3136
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6808
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9978
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1180
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 448
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.53e1

InbreedingCoeff
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MQ
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DP
type: SiteQuality
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MQRankSum
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FS
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 216
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3192
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6820
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 192
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.162e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

DP
type: SiteQuality
SIO_000300: 4.27677e5

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.98e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

GenotypeQuality
all individuals: 78
bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 512
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3682
num of homozygotes: 0

European (Finnish)
type: Population
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: 1892
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12226
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7330
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

VQSLOD
type: SiteQuality
SIO_000300: 3.16e0

DP
type: SiteQuality
SIO_000300: 4.98815e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.76e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.275e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 2141
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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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: 7.5e0
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 8.25e1
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GenotypeQuality
all individuals: 80
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3790
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 210
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7474
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 5.030181086519115e-4
allele num: 1988
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12692
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.121e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.59e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.451000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-2

DP
type: SiteQuality
SIO_000300: 5.10368e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.12e-1

QD
type: SiteQuality
SIO_000300: 1.656e1

GenotypeQuality
all individuals: 962
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1018
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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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

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.196315486470927e-5
allele num: 13896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4010
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2368
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.1e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.21e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.33e-1

DP
type: SiteQuality
SIO_000300: 5.41117e5

VQSLOD
type: SiteQuality
SIO_000300: -4.871e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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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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GenotypeQuality
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GenotypeQuality
all individuals: 346
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GenotypeQuality
all individuals: 69
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4048
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2398
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7770
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14124
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

FS
type: SiteQuality
SIO_000300: 3.638e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.14e-2

DP
type: SiteQuality
SIO_000300: 5.47051e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

QD
type: SiteQuality
SIO_000300: 7.49e0

VQSLOD
type: SiteQuality
SIO_000300: -1.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 457
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GenotypeQuality
all individuals: 1153
bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2682
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8048
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.545359340227778e-5
allele num: 15278
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-2

DP
type: SiteQuality
SIO_000300: 5.73991e5

FS
type: SiteQuality
SIO_000300: 5.545e0

MQRankSum
type: SiteQuality
SIO_000300: 7.84e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.172e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.81e-2

QD
type: SiteQuality
SIO_000300: 6.24e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1